Patent Application
20090270645
The invention relates to a process for extractively removing nickel(0) complexes having phosphorus ligands from a reaction effluent of a hydrocyanation of unsaturated mononitriles to dinitriles by extraction by means of a hydrocarbon, wherein a phase separation of the hydrocarbon and of the nitrile-containing solution into two phases is effected and a polar additive is added to the hydrocyanation effluent (feed stream) and/or to the extraction stage.
For hydrocyanations of unsaturated mononitriles, nickel complexes of phosphorus ligands are suitable catalysts. For example, adiponitrile, an important intermediate in nylon production, is prepared by double hydrocyanation of 1,3-butadiene. In a first hydrocyanation, 1,3-butadiene is reacted with hydrogen cyanide in the presence of nickel(0) which is stabilized with phosphorus ligands to give 3-pentenenitrile. In a second hydrocyanation 1,3-pentenenitrile is then reactive with hydrogen cyanide to give adiponitrile, likewise over a nickel catalyst, but if appropriate with addition of a Lewis acid and possibly of a promoter. Nickel(0) or Ni(0) means nickel in the 0 oxidation state.
In order to increase the economic viability of the hydrocyanation, the nickel catalyst is typically removed and recycles (catalyst circuit). Since the catalyst system in the second hydrocyanation, which is a mixture of complex and free ligands, cannot be thermally stressed to a high degree, the high-boiling adiponitrile cannot be removed from the catalyst system by distillation. The separation is therefore generally carried out extractively with hydrocarbons as extractants. The catalyst system remains, ideally fully, under real conditions at least partly, in the lighter hydrocarbon phase, while the heavier phase is more polar and comprises crude adiponitrile, the predominant portion of the unconverted pentenenitrile and the Lewis acid. After the phase separation, the extractant is generally removed from the catalyst system by distillation under reduced pressure, pentenenitriles being added for dilution. The boiling pressure of the extractant is significantly higher than that of the pentenenitriles.
U.S. Pat. No. 3,773,809 and 5,932,772 describes the extraction of the catalyst complex and of the ligands with paraffins and cycloparaffins, for example cyclohexane, heptane and octane, or alkylaromatics.
U.S. Pat. No. 4,339,395 discloses a process for extractive workup of reaction effluents from hydrocyanations for catalyst systems with monodentate ligands and a triarylborane as promoter, in which a small amount of ammonia is metered in to prevent rag formation.
WO 2004/062765 describes the extractive removal of a nickel diphosphite catalyst from a mixture of mono- and dinitriles with alkanes or cycloalkanes as the extractant, the mixture being treated with a Lewis base, for example organoamines or ammonia.
U.S. Pat. No. 5,847,191 discloses a process for extractive workup of reaction effluents of hydrocyanations, the chelate ligands bearing C9- to C40-alkyl radicals.
U.S. Pat. No. 4,990,645 states that the extractability of the nickel complex and of the free ligand can be improved when the Ni(CN)2 solid formed in the reaction is removed in a decanter before the extraction. To this end, some of the pentenenitrile is evaporated off beforehand in order to reduce the solubility of the catalyst and of the Ni(CN)2.
In order to achieve a phase separation between the hydrocarbon-containing phase and the crude adiponitrile-containing phase, it has hitherto been necessary to achieve a minimum conversion of the 3-pentenenitrile. Thus, U.S. Pat. No. 3,773,809 requires, as a condition for the phase separation in the case of use of cyclohexane as an extractant, a minimum conversion of 3-pntenenitrile of 60%, so that the ratio between 3-pentenenitrile and adiponitrile is below 0.65. When this ratio is not achieved by converting 3-pentenenitrile, it is necessary either to preevaporate 3-pentenenitrile or to add adiponitrile in order to arrive at a ratio of below 0.65. A problem with this minimum conversion of 3-pentenenitrile is that a poor selectivity of adiponitrile for 3-pentenenitrile and hydrogen cyanide is associated with a higher conversion of 3-pentenenitrile. Moreover, a minimum conversion of 3-pentenenitrile of 60% leads to a short lifetime of the catalyst system.
High demands are made on a continuous industrial scale extraction. Nickel(0) complexes and phosphorus ligands should be depleted down to small residual amounts from a large feed stream. The problems which occur include lag formation at the phase interfaces and the formation of solids which are deposited on the extraction apparatus and can thus lead, for example, to the sticking of solids on internals and narrowing of column cross sections.
It was therefore an object of the present invention to remedy the aforementioned disadvantages, i.e. to provide a process for extractively removing nickel(0) complexes having phosphorus ligands and/or free phosphorus ligands from a reaction effluent of a hydrocyanation of unsaturated mononitriles to dinitriles, which avoids the above-described disadvantages of the known processes.
In particular, it should be possible in the process according to the invention to suppress rag formation and the deposition of solids and/or to increase their rapidity of phase separation and, if appropriate, to operate the continuous extraction largely without disruption over a prolonged period.
Accordingly, the process mentioned at the outset has been found. Preferred embodiments of the invention can be taken from the subclaims.
In a particularly preferred embodiment, the process according to the invention is used in the preparation of adiponitrile. The process according to the invention is thus preferably intended for 3-pentenenitrile as the mononitrile and adiponitrile as the dinitrile. The reaction effluent of the hydrocyanation is likewise preferably obtained by reacting 3-pentenenitrile with hydrogen cyanide in the presence of at least one nickel(0) complex having phosphorus ligands, if appropriate in the presence of at least one Lewis acid (for example as a promoter).
The process according to the invention is suitable for extractively removing Ni(0) complexes which comprise phosphorus ligands and/or free phosphorus ligands from a reaction effluent which is obtained in a hydrocyanation of unsaturated mononitriles to dinitriles. These complexes are described below.
The reaction effluent from which, if appropriate, a portion or the entire amount of unconverted pentenenitriles has been removed is extracted by means of a hydrocarbon with addition of a polar additive; in the course of this, a phase separation of the hydrocarbon and of the reaction effluent into two phases occurs. In general, a first phase which is enriched in the Ni(0) complexes or ligands mentioned compared to the reaction effluent, and a second phase which is enriched in dinitriles compared to the reaction effluent, are formed. Usually, the first phase is the lighter phase, i.e. the upper phase, and the second phase the heavier phase, i.e. the lower phase.
Depending on the phase ratio, the extraction has an extraction coefficient, defined as the ratio of the mass content of the nickel(0) complexes or ligands mentioned in the upper phase to the mass content of the nickel(0) complexes or ligands mentioned in the lower phase, for each theoretical extraction stage of preferably from 0.1 to 50, more preferably from 0.6 to 30.
After the phase separation, the upper phase contains preferably between 50 and 99% by weight, more preferably between 60 and 97% by weight, in particular between 80 and 95% by weight, of the hydrocarbon used for the extraction.
The Lewis acid which is, if appropriate (specifically in the second hydrocyanation mentioned at the outset), present in the feed stream of the extraction remains preferably for the most part and more preferably fully in the lower phase. Here, fully means that the residual concentration of the Lewis acid in the upper phase is preferably less than 1% by weight, more preferably less than 0.5% by weight, in particular less than 500 ppm by weight.
The hydrocarbon is the extractant. It has a boiling point of preferably at least 30° C., more preferably at least 60° C., in particular at least 90° C., and preferably at most 140° C., more preferably at most 135° C., in particular at most 130° C., based in each case on a pressure of 105 Pa absolute.
A hydrocarbon, this referring in the context of the present invention either to an individual hydrocarbon or to a mixture of such hydrocarbons, can more preferably be used for the removal, especially by extraction, of adiponitrile from a mixture comprising adiponitrile and the Ni(0)-containing catalyst, said hydrocarbon having a boiling point in the range between 60° C. and 135° C. The catalyst, if appropriate with addition of a suitable solvent which is higher-boiling than the hydrocarbon H (e.g. pentenenitrile), may advantageously be obtained by distillative removal of the hydrocarbon from the mixture obtained after the removal by this process, in which case the use of a hydrocarbon having a boiling point in the range specified permits a particularly economically viable and technically simple removal as a result of the possibility of condensing the hydrocarbon distilled off with river water.
Suitable hydrocarbons are described, for example, in U.S. Pat. No. 3,773,809, column 3, lines 50-62. Preference is given to a hydrocarbon selected from cyclohexane, methylcyclohexane, cycloheptane, n-hexane, n-heptane, isomeric heptanes, n-octane, isooctane, isomeric octanes such as 2,2,4-trimethylpentane, cis- and trans-decalin or mixtures thereof, especially of cyclohexane, methylcyclohexane, n-heptane, isomeric heptanes, n-octane, isomeric octanes such as 2,2,4-trimethylpentane, or mixtures thereof. Particular preference is given to using cyclohexane, methylcyclohexane, n-heptane or n-octane.
Very particular preference is given to n-heptane or n-octane. With these hydrocarbons, the undesired rag formation is particularly low. Rag refers to a region of incomplete phase separation between upper and lower phase, usually a liquid/liquid mixture in which solids may also be dispersed. Excess rag formation is undesired since it hinders the extraction and the extraction apparatus can under some circumstances be flooded by rag, as a result of which it can no longer fulfill its separation task.
The hydrocarbon used is preferably anhydrous, anhydrous meaning a water content of below 100 ppm by weight, preferably below 50 ppm by weight, in particular below 10 ppm by weight. The hydrocarbon may be dried by suitable processes known to those skilled in the art, for example by adsorption or azeotropic distillation. The drying may be effected by a step preceding the process according to the invention.
The objects mentioned at the outset are achieved by a process for extractively removing nickel(0) complexes having phosphorus ligands and/or free phosphorus ligands from a reaction effluent of a hydrocyanation of unsaturated mononitriles to dinitriles by extraction by means of a hydrocarbon, a phase separation of the hydrocarbon and of the reaction effluent into two phases being effected, by virtue of addition of at least one polar additive to the hydrocyanation effluent reducing rag and/or solids formation and increasing the rapidity of phase separation.
Polar additives are understood to mean organic compounds which, by increasing the polarity of the dinitrile phase, bring about accelerated phase separation and reduced rage and solids formation.
Suitable polar additives are in particular saturated linear or branched aliphatic nitrites having from two to ten carbon atoms and aromatic nitriles having from seven to twelve carbon atoms.
Examples thereof are acetonitrile, propionitrile, butyronitrile, 2-methylbutanenitrile, pentanenitrile, hexanenitrile, heptanenitrile and octanenitrile, cyclohexanenitrile, benzonitrile and alkylbenzonitrile such as 2-methylbenzonitrile and 2-ethylbenzonitrile, or mixtures of these compounds.
Preference is given to saturated aliphatic nitrites having from two to six carbon atoms or mixtures of these compounds. Particular preference is given to acetonitrile.
Also suitable are sulfolane, alkylureas and pyrrolidones. Examples thereof are dimethylurea, tetraethylurea, tetramethylurea, pyrrolidone, N-methylpyrrolidone, N-ethylpyrrolidone, N-hexylpyrrolidone or mixtures of these compounds.
Configuration of the extraction in the presence of polar additives The extraction of the nickel(0) complexes or ligands from the reaction effluent may be carried out in any suitable apparatus known to those skilled in the art, preferably in countercurrent extraction columns, mixer-settler units or combinations of mixer-settler units with columns. Particular preference is given to the use of countercurrent extraction columns which are equipped in particular with sheet metal packings as dispersing elements. In a further particularly preferred embodiment, the extraction is performed in countercurrent in a compartmented, stirred extraction column (for example a rotating-disk contactor (RDC), Kühni column, Scheibel column, QVF column).
Regarding the dispersion direction, in a preferred embodiment of the process, the hydrocarbon is used as the continuous phase and the reaction effluent of the hydrocyanation as the disperse phase. This generally also shortens the phase separation time and reduces rag formation. However, the reverse dispersion direction is also possible, i.e. reaction effluent as the continuous and hydrocarbon as the disperse phase. The latter is especially true when the rag formation is reduced or suppressed fully by preceding solids removal (see below), higher temperatures in the extraction or phase separation or use of a suitable hydrocarbon. Typically, the dispersion direction more favorable for the separating performance of the extraction apparatus is selected.
The extractant, the polar additive and the feed stream can be fed to the extraction apparatus separately or together.
In the extraction, a phase ratio of preferably from 0.1 to 10, more preferably from 0.4 to 3, in particular from 0.75 to 1.5, calculated in each case as the ratio of mass of the hydrocarbon supplied to mass of the mixture to be extracted, is used.
The mass of polar additive is from 1 to 50% by weight, preferably from 2 to 45% by weight, more preferably from 3 to 40% by weight, based on the mass of the feed stream.
The absolute pressure during the extraction is preferably from 10 kPa to 1 MPa, more preferably from 50 kPa to 0.5 MPa, in particular from 75 kPa to 0.25 MPa (absolute).
The extraction is preferably carried out at a temperature of −15 to 120° C., in particular from 20 to 100° C. and more preferably from 30 to 80° C. It has been found that the rag formation is lower at relatively high temperature of the extraction.
In a particularly preferred embodiment, the extraction is operated with a temperature profile. In particular, operation is effected in this case at an extraction temperature of at least 30° C., preferably from 30 to 95° C. and more preferably at least 40° C.
The temperature profile is preferably configured in such a way that, in that region of the extraction in which the content of nickel(0) complexes having phosphorus ligands and/or free phosphorus ligands is higher than in the other region, the temperature is lower than the other region. In this way, the thermally labile Ni(0) complexes are less thermally stressed and their decomposition is reduced.
Configuration of the phase separation in the presence of polar additives
Depending on the apparatus configuration, the phase separation may also be viewed in spatial terms and in terms of time as the last part of the extraction. For the phase separation, a wide pressure, concentration and temperature range may typically be selected, and the optimal parameters for the particular composition of the reaction mixture can be determined readily by a few simple preliminary experiments.
The temperature T in the phase separation is typically at least 0° C., preferably at least 10° C., more preferably at least 20° C. Typically, it is at most 80° C., preferably at most 70° C., more preferably at most 60° C. For example, the phase separation is carried out at from 10 to 80° C., preferably from 20 to 70° C. It has been found that the rag formation is lower at relatively high temperature of the phase separation.
The pressure in the phase separation is generally at least 1 kPa, preferably at least 10 kPa, more preferably 20 kPa. In general, it is at most 2 MPa, preferably at most 1 MPa, more preferably at most 0.5 MPa absolute.
The phase separation may be carried out in one or more apparatuses known to those skilled in the art for such phase separations. In an advantageous embodiment, the phase separation may be carried out in the extraction apparatus, for example in one or more mixer-settler combinations or by equipping an extraction column with a calming zone.
In the hydrocarbon phase, the full retention of the entrained phase fraction of heavy AND phase may be advantageous. In this case, normal gravitational separation in a simple settler is not sufficient. Depending on the degree of the desired separation, it is possible here to use a gravitational separator with internals as coalescence aids (for example lamellae, fabric packings or sheet metal packings), a cyclone separator, or, in the extreme case that the heavy phase is to be retained fully, a mechanically driven centrifugal separator (for example plate separator).
In the disperse phase, the rag phase can, should it not be possible to entirely suppress rage accumulation in the phase separator, be removed selectively from the settler. In certain cases, it is also sufficient to establish a certain controlled layering of the continuous phase together with the disperse.
The phase separation affords two liquid phases of which one phase has a higher content of the nickel(0) complex having phosphorus ligands and/or free phosphorus ligands, based on the total weight of this phase, than the other phase or the other phases.
The phase comprising the higher content of Ni(0) complexes and phosphorus ligands can, if appropriate after regeneration of the catalyst and removal of the extractant, be recycled into the hydrocyanation stage.
The phase comprising predominantly dinitrile, unconverted mononitrile and polar additive can be separated by distillation.
When the polar additive has the lowest boiling point of the compounds present, it can be removed as the top product in a first column, with mononitrile and dinitrile as the bottom product. In a second column, the bottom product of the first column can be separated such that the mononitrile is removed via the top and the dinitrile via the bottom. However, it is also possible to perform the separation in only one column and in this case to remove the polar additive via the top, mononitrile Via a side drawer and dinitrile via the bottom.
When the mononitrile has the lowest boiling point, it can be removed via the top, and the polar additive via side drawer removal, or, in the case of two-stage distillation, together with dinitrile via the bottom.
The dinitrile product of value can be discharged from the process, and mononitrile can be recycled into the hydrocyanation and polar additive into the extraction.
It is also possible to remove mononitrile and polar additive as a mixture and recycle them into the hydrocyanation.
The amount of polar additive is generally from 1 to 50% by weight, preferably from 2 to 45% by weight, based on the amount of the feed stream.
Optional Treatment with Ammonia or Amine
In a preferred embodiment of the process according to the invention, the reaction effluent of the hydrocyanation is treated before or during the extraction with ammonia or a primary, secondary or tertiary, aromatic or aliphatic amine. Aromatic includes alkylaromatic, and aliphatic includes cycloaliphatic.
It has been found that this ammonia or amine treatment can reduce the content of nickel(0) complex or ligand in the second phase enriched with dinitriles (usually lower phase), i.e. the distribution of Ni(0) complex or ligand between the two phases is shifted in favor of the first phase (upper phase). The ammonia or amine treatment improves the catalyst enrichment in the upper phase; this means lower catalyst losses in the catalyst cycle and increases the economic viability of the hydrocyanation. Accordingly, in this embodiment, the extraction is preceded by a treatment of the reaction effluent with ammonia or an amine or this is effected during the extraction. The treatment during the extraction is less preferred.
The amines used are monoamines, diamines, triamines or more highly functional amines (polyamines). The monoamines typically have alkyl radicals, aryl radicals or arylalkyl radicals having from 1 to 30 carbon atoms; suitable monoamines are, for example, primary amines, e.g. monoalkylamines, secondary or tertiary amines, e.g. dialkylamines. Suitable primary monoamines are, for example, butylamine, cyclohexylamine, 2-methylcyclohexylamine, 3-methylcyclohexylamine, 4-methylcyclohexylamine, benzylamine, tetrahydrofurfurylamine and furfurylamine. Useful secondary monoamines are, for example, diethylamine, dibutylamine, di-n-propylamine and N-methylbenzylamine. Suitable tertiary amines are, for example, trialkylamines having C1-10 alkyl radicals such as trimethylamine, triethylamine or tributylamine.
Suitable diamines are, for example, those of the formula R1—NH—R2—NH—R3, where R1, R2 and R3 are each independently hydrogen or an alkyl radical, aryl radical or arlalkyl radical having from 1 to 20 carbon atoms. The alkyl radical may be linear or, especially for R2, also cyclic. Suitable diamines are, for example, ethylenediamine, propylenediamines (1,2-diaminopropane and 1,3-diaminopropane), N-methyl-ethylenediamine, piperazine, tetramethylenediamine (1,4-diaminobutane), N,N′-dimethylethylenediamine; N-ethylethylenediamine, 1,5-diaminopentane, 1,3-diamino-2,2-diethylpropane, 1,3-bis(methylamino)propane, hexamethylenediamine (1,6-diaminohexane), 1,5-diamino-2-methylpentane, 3-(propylamino)propylamine, N,N′-bis(3-aminopropyl)piperazine, N,N′-bis(3-aminopropyl)piperazine and isophoronediamine (IPDA).
Suitable triamines, tetramines or more highly functional amines are, for example, tris(2-aminoethyl)amine, tris(2-aminopropyl)amine, diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), isopropylenetriamine, dipropylenetriamine and N,N′-bis(3-aminopropylethylenediamine). Aminobenzylamines and aminohydrazides having 2 or more amino groups are likewise suitable.
Of course, it is also possible to use mixtures of ammonia with one or more amines, or mixtures of a plurality of amines.
Preference is given to using ammonia or aliphatic amines, in particular trialkylamines having from 1 to 10 carbon atoms in the alkyl radical, for example trimethylamine, triethylamine or tributylamine, and also diamines such as ethylenediamine, hexa-methylenediamine or 1,5-diamino-2-methylpentane.
Particular preference is given to ammonia alone; in other words, particular preference is given to using no amine apart from ammonia. Very particular preference is given to anhydrous ammonia; in this case, anhydrous means a water content below 1% by weight, preferably below 1000 ppm by weight and in particular below 100 ppm by weight.
The molar ratio of amine to ammonia may be varied within wide limits, and is generally from 10 000:1 to 1:10 000.
The amount of the ammonia or amine used depends, inter alia, on the type and amount of the nickel(0) catalyst and/or of the ligands and, if used, on the type and amount of the Lewis acid which is used as a promoter in the hydrocyanation. Typically, the molar ratio of ammonia or amine to Lewis acid is at least 1:1. The upper limit of this molar ratio is generally uncritical and is, for example, 100:1; however, the excess of ammonia or amine should not be so great that the Ni(0) complex or its ligand decomposes. The molar ratio of ammonia or amine to Lewis acid is preferably from 1:1 to 10:1, more preferably from 1.5:1 to 5:1, and in particular about 2.0:1. When a mixture of ammonia and amine is used, these molar ratios apply to the sum of ammonia and amine.
The temperature in the treatment with ammonia or amine is typically not critical and is, for example, from 10 to 140° C., preferably from 20 to 100° C. and in particular from 20 to 90° C. The pressure is generally not critical either.
The ammonia or the amine may be added to the reaction effluent in gaseous form, in liquid form (under pressure) or dissolved in a solvent. Suitable solvents are, for example, nitrites, especially those which are present in the hydrocyanation, and also aliphatic, cycloaliphatic or aromatic hydrocarbons, as used in the process according to the invention as extractants, for example cyclohexane, methylcyclohexane, n-heptane or n-octane.
The ammonia or amine addition is effected in customary apparatus, for example those for gas introduction or in liquid mixers. The solid which precipitates out in many cases may either remain in the reaction effluent, i.e. a suspension is fed to the extraction, or be removed as described below.
In a preferred embodiment, the solids present in the reaction effluent are removed at least partly before the extraction. In many cases, this allows the extraction performance of the process according to the invention to be improved further. It is suspected that a high solids content hinders the mass transfer during the extraction, which makes necessary larger and thus more expensive extraction apparatus. It has also been found that the solids removal before the extraction often distinctly reduces the undesired rag formation.
Preference is given to configuring the solids removal in such a way that the solid particles having a hydraulic diameter of greater than 5 μm, in particular greater than 1 μm and more preferably greater than 100 nm are removed.
For the solids removal, it is possible to use customary processes, for example filtration, crossflow filtration, centrifugation, sedimentation, classification or preferably decantation, for which common apparatus such as filters, centrifuges and decanters can be used.
Temperature and pressure in the solids removal are typically not critical. For example, it is possible to work within the aforementioned temperature and pressure ranges.
The solids removal may be effected before, during or after the optional treatment of the reaction effluent with ammonia or amine. The removal is preferably during or after the ammonia or amine treatment, more preferably thereafter.
When the solids are removed during or after the amine or ammonia treatment, the solids are usually compounds of ammonia or amine with the Lewis acid or the promoter, used which are sparingly soluble in the reaction effluent. When, for example, ZnCl2 is used, substantially sparingly soluble ZnCl2.2NH3 is formed in the ammonia treatment.
When the solids are removed before the ammonia or amine treatment, or if there is no treatment with ammonia or amine at all, the solids are generally nickel compounds of the +II oxidation state, for example nickel(II) cyanide or similar cyanide-containing nickel(II) compounds.
The Ni(0) complexes which comprise phosphorus ligands and/or free phosphorus ligands are preferably homogeneously dissolved nickel(0) complexes.
The phosphorus ligands of the nickel(0) complexes and the free phosphorus ligands, which are removed by extraction in accordance with the invention, are preferably selected from mono- or bidentate phosphines, phosphites, phosphinites and phosphonites.
These phosphorus ligands preferably have the formula I:
P(X1R1)(X2R2)(X3R3) (I).
In the context of the present invention, compound I is a single compound or a mixture of different compounds of the aforementioned formula.
According to the invention, X1, X2, X3 each independently are oxygen or a single bond. When all of the X1, X2 and X3 groups are single bonds, compound I is a phosphine of the formula P(R1R2R3) with the definitions of R1, R2 and R3 specified in this description.
When two of the X1, X2 and X3 groups are single bonds and one is oxygen, compound I is a phosphinite of the formula P(OR1)(R2)(R3) or P(R1)(OR2)(R3) or P(R1)(R2)(OR3) with the definitions of R1, R2 and R3 specified in this description.
When one of the X1, X2 and X3 groups is a single bond and two are oxygen, compound I is a phosphonite of the formula P(OR1)(OR2)(R3) or P(R1)(OR2)(OR3) or P(OR1)(R2)(OR3) with the definitions of R1, R2 and R3 specified in this description.
In a preferred embodiment, all X1, X2 and X3 groups should be oxygen, so that compound I is advantageously a phosphite of the formula P(OR1)(OR2)(OR3) with the definitions of R1, R2 and R3 specified in this description.
According to the invention, R1, R2, R3 are each independently identical or different organic radicals. R1, R2 and R3 are each independently alkyl radicals preferably having from 1 to 10 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, aryl groups such as phenyl, o-tolyl, m-tolyl, p-tolyl, 1-naphthyl, 2-naphthyl, or hydrocarbyl, preferably having from 1 to 20 carbon atoms, such as 1,1′-biphenol, 1,1′-binaphthol. The R1, R2 and R3 groups may be bonded together directly, i.e. not solely via the central phosphorus atom. Preference is given to the R1, R2 and R3 groups not being bonded together directly.
In a preferred embodiment, R1, R2 and R3 groups are radicals selected from the group consisting of phenyl, o-tolyl, m-tolyl and p-tolyl. In a particularly preferred embodiment, a maximum of two of the R1, R2 and R3 groups should be phenyl groups.
In another preferred embodiment, a maximum of two of the R1, R2 and R3 groups should be o-tolyl groups.
Particularly preferred compounds I which may be used are those of the formula Ia
(o-tolyl-O—)w(m-tolyl-O—)x(p-tolyl-O—)y(phenyl-O—)zP (Ia)
where w, x, y, z are each a natural number where w+x+y+z=3 and w, z≦2.
Such compounds I a are, for example, (p-tolyl-O—)(phenyl-O—)2P, (m-tolyl-O—)(phenyl-O—)2P, (o-tolyl-O—)(phenyl-O—)2P, (p-tolyl-O—)2(phenyl-O—)P, (m-tolyl-O—)2(phenyl-O—)P, (o-tolyl-O—)2(phenyl-O—)P, (m-tolyl-O—)(p-tolyl-O—)(phenyl-O—)P, (o-tolyl-O—)(p-tolyl-O—)(phenyl-O—)P, (o-tolyl-O—) (m-tolyl-O—)(phenyl-O—)P, (p-tolyl-O—)3P, (m-tolyl-O—)(p-tolyl-O—)2P, (o-tolyl-O—)(p-tolyl-O—)2P, (m-tolyl-O—)2(p-tolyl-O—)P, (o-tolyl-O—)2(p-tolyl-O—)P, (o-tolyl-O—)(m-tolyl-O—) (p-tolyl-O—)P, (m-tolyl-O—)3P, (o-tolyl-O—)(m-tolyl-O—)2P, (o-tolyl-O—)2(m-tolyl-O—)P or mixtures of such compounds.
For example, mixtures comprising (m-tolyl-O—)3P, (m-tolyl-O—)2(p-tolyl-O—)P, (m-tolyl-O—)(p-tolyl-O—)2P and (p-tolyl-O—)3P may be obtained by reacting a mixture comprising m-cresol and p-cresol, in particular in a molar ratio of 2:1, as obtained in the distillative workup of crude oil, with a phosphorus trihalide, such as phosphorus tri-chloride.
In another, likewise preferred embodiment, the phosphorus ligands are the phosphites, described in detail in DE-A 199 53 058, of the formula I b:
P(O—R1)x(O—R2)y(O—R3)z(O—R4)p (I b)
where
Preferred phosphites of the formula I b can be taken from DE-A 199 53 058. The R1 radical may advantageously be o-tolyl, o-ethylphenyl, o-n-propylphenyl, o-isopropyl-phenyl, o-n-butylphenyl, o-sec-butylphenyl, o-tert-butylphenyl, (o-phenyl)phenyl or 1-naphthyl groups.
Preferred R2 radicals are m-tolyl, m-ethylphenyl, m-n-propylphenyl, m-isopropylphenyl, m-n-butylphenyl, m-sec-butylphenyl, m-tert-butylphenyl, (m-phenyl)phenyl or 2-naphthyl groups.
Advantageous R3 radicals are p-tolyl, p-ethylphenyl, p-n-propylphenyl, p-isopropyl-phenyl, p-n-butylphenyl, p-sec-butylphenyl, p-tert-butylphenyl or (p-phenyl)phenyl groups.
The R4 radical is preferably phenyl. p is preferably zero. For the indices x, y and z and p in compound I b, there are the following possibilities:
Preferred phosphites of the formula I b are those in which p is zero, and R1, R2 and R3 are each independently selected from o-isopropylphenyl, m-tolyl and p-tolyl, and R4 is phenyl, Particularly preferred phosphates of the formula I b are those in which R1 is the o-isopropylphenyl radical, R2 is the m-tolyl radical and R3 is the p-tolyl radical with the indices specified in the table above; also those in which R1 is the o-tolyl radical, R2 is the m-tolyl radical and R3 is the p-tolyl radical with the indices specified in the table; additionally those in which R1 is the 1-naphthyl radical, R2 is the m-tolyl radical and R3 is the p-tolyl radical with the indices specified in the table; also those in which R1 is the o-tolyl radical, R2 is the 2-naphthyl radical and R3 is the p-tolyl radical with the indices specified in the table; and finally those in which R1 is the o-isopropylphenyl radical, R2 is the 2-naphthyl radical and R3 is the p-tolyl radical with the indices specified in the table; and also mixtures of these phosphites.
Phosphites of the formula I b may be obtained by
The reaction may be carried out in three separate steps. Equally, two of the three steps may be combined, i.e. a) with b) or b) with c). Alternatively, all of steps a), b) and c) may be combined together.
Suitable parameters and amounts of the alcohols selected from the group consisting of R1OH, R2OH, R3OH and R4OH or mixtures thereof may be determined readily by a few simple preliminary experiments.
Useful phosphorus trihalides are in principle all phosphorus trihalides, preferably those in which the halide used is Cl, Br, I, in particular Cl, and mixtures thereof. It is also possible to use mixtures of identically or differently halogen-substituted phosphines as the phosphorus trihalide. Particular preference is given to PCl3. Further details on the reaction conditions in the preparation of the phosphites I b and for the workup can be taken from DE-A 199 53 058.
The phosphites I b may also be used in the form of a mixture of different phosphites I b as a ligand. Such a mixture may be obtained, for example, in the preparation of the phosphites I b.
However, preference is given to the phosphorus ligand being multidentate, in particular bidentate. The ligand used therefore preferably has the formula II
where
In the context of the present invention, compound II is a single compound or a mixture of different compounds of the aforementioned formula.
In a preferred embodiment, X11, X12, X13, X21, X22, X23 may each be oxygen. In such a case, the bridging group Y is bonded to phosphite groups.
In another preferred embodiment, X11 and X12 may each be oxygen and X13 a single bond, or X11 and X13 each oxygen and X12 a single bond, so that the phosphorus atom surrounded by X11, X12 and X13 is the central atom of a phosphonite. In such a case, X21, X22 and X23 may each be oxygen, or X21 and X22 may each be oxygen and X23 a single bond, or X21 and X23 may each be oxygen and X22 a single bond, or X23 may be oxygen and X21 and X22 each a single bond, or X21 may be oxygen and X22 and X23 each a single bond, or X21, X22 and X23 may each be a single bond, so that the phosphorus atom surrounded by X21, X22 and X23 may be the central atom of a phosphite, phosphonite, phosphinite or phosphine, preferably a phosphonite.
In another preferred embodiment, X13 may be oxygen and X11 and X12 each a single bond, or X11 may be oxygen and X12 and X13 each a single bond, so that the phosphorus atom surrounded by X11, X12 and X13 is the central atom of a phosphonite. In such a case, X21, X22 and X23 may each be oxygen, or X23 may be oxygen and X21 and X22 each a single bond, or X21 may be oxygen and X22 and X23 each a single bond, or X21, X22 and X23 may each be a single bond, so that the phosphorus atom surrounded by X21, X22 and X23 may be the central atom of a phosphite, phosphinite or phosphine, preferably a phosphinite.
In another preferred embodiment, X11, X12 and X13 may each be a single bond, so that the phosphorus atom surrounded by X11, X12 and X13 is the central atom of a phosphine. In such a case, X21, X22 and X23 may each be oxygen, or X21, X22 and X23 may each be a single bond, so that the phosphorus atom surrounded by X21, X22 and X23 may be the central atom of a phosphite or phosphine, preferably a phosphine.
The bridging group Y is preferably an aryl group which is substituted, for example by C1-C4-alkyl, halogen, such as fluorine, chlorine, bromine, halogenated alkyl, such as trifluoromethyl, aryl, such as phenyl, or is unsubstituted, preferably a group having from 6 to 20 carbon atoms in the aromatic system, in particular pyrocatechol, bis(phenol) or bis(naphthol).
The R11 and R12 radicals may each independently be identical or different organic radicals. Advantageous R11 and R12 radicals are aryl radicals, preferably those having from 6 to 10 carbon atoms, which may be unsubstituted or mono- or polysubstituted, in particular by C1-C4-alkyl, halogen, such as fluorine, chlorine, bromine, halogenated alkyl, such as trifluoromethyl, aryl, such as phenyl, or unsubstituted aryl groups.
The R21 and R22 radicals may each independently be identical or different organic radicals. Advantageous R21 and R22 radicals are aryl radicals, preferably those having from 6 to 10 carbon atoms, which may be unsubstituted or mono- or polysubstituted, in particular by C1-C4-alkyl, halogen, such as fluorine, chlorine, bromine, halogenated alkyl, such as trifluoromethyl, aryl, such as phenyl, or unsubstituted aryl groups.
The R11 and R12 radicals may each be separate or bridged. The R21 and R22 radicals may also each be separate or bridged. The R11, R12, R21 and R22 radicals may each be separate, two may be bridged and two separate, or all four may be bridged, in the manner described.
In a particularly preferred embodiment, useful compounds are those of the formula I, II, III, IV and V specified in U.S. Pat. No. 5,723,641. In a particularly preferred embodiment, useful compounds are those of the formula I, II, III, IV, V, VI and VII specified in U.S. Pat. No. 5,512,696, in particular the compounds used there in examples 1 to 31. In a particularly preferred embodiment, useful compounds are those of the formula I, II, II, IV, V, VI, VII, VIII, IX, X, XI, XII, XIII, XIV and XV specified in U.S. Pat. No. 5,821,378, in particular the compounds used there in examples 1 to 73.
In a particularly preferred embodiment, useful compounds are those of the formula I, II, III, IV, V and VI specified in U.S. Pat. No. 5,512,695, in particular the compounds used there in examples 1 to 6. In a particularly preferred embodiment, useful compounds are those of the formula I, II, III, IV, V, VI, VII, VIII, IX, X, XI, XII, XIII and XIV specified in U.S. Pat. No. 5,981,772, in particular the compounds used there in examples 1 to 66.
In a particularly preferred embodiment, useful compounds are those specified in U.S. Pat. No. 6,127,567 and the compounds used there in examples 1 to 29. In a particularly preferred embodiment, useful compounds are those of the formula I, II, III, IV, V, VI, VII, VIII, IX and X specified in U.S. Pat. No. 6,020,516, in particular the compounds used there in examples 1 to 33. In a particularly preferred embodiment, useful compounds are those specified in U.S. Pat. No. 5,959,135, and the compounds used there in examples 1 to 13. In a particularly preferred embodiment, useful compounds are those of the formula I, II and III specified in U.S. Pat. No. 5,847,191. In a particularly preferred embodiment, useful compounds are those specified in U.S. Pat. No. 5,523,453, in particular the compounds illustrated there in formula 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, and 21. In a particularly preferred embodiment, useful compounds are those specified in WO 01/14392, preferably the compounds illustrated there in formula V, VI, VII, VIII, IX, X, XI, XII, XIII, XIV, XV, XVI, XVII, XXI, XXII, XXIII.
In a particularly preferred embodiment, useful compounds are those specified in WO 98/27054. In a particularly preferred embodiment, useful compounds are those specified in WO 99/13983. In a particularly preferred embodiment, useful compounds are those specified in WO 99/64155.
In a particularly preferred embodiment, useful compounds are those specified in the German patent application DE 100 380 37. In a particularly preferred embodiment, useful compounds are those specified in the German patent application DE 100 460 25. In a particularly preferred embodiment, useful compounds are those specified in the German patent application DE 101 502 85.
In a particularly preferred embodiment, useful compounds are those specified in the German patent application DE 101 502 86. In a particularly preferred embodiment, useful compounds are those specified in the German patent application DE 102 071 65. In a further particularly preferred embodiment of the present invention, useful phosphorus chelate ligands are those specified in US 2003/0100442 A1.
In a further particularly preferred embodiment of the present invention, useful phosphorus chelate ligands are those specified in the German patent application of reference number DE 103 50 999.2 of 10.30.2003, which has an earlier priority date but had not been published at the priority date of the present application.
The compounds I, I a, I b and II described and their preparation are known per se. The phosphorus ligands used may also be mixtures comprising at least two of the compounds I, I a, I b and II.
In a particularly preferred embodiment of the process according to the invention, the phosphorus ligand of the nickel(0) complex and/or the free phosphorus ligand is selected from tritolyl phosphite, bidentate phosphorus chelate ligands and the phosphites of the formula I b
P(O—R1)x(O—R2)y(O—R3)z(O—R4)p (I b)
where R1, R2 and R3 are each independently selected from o-isopropylphenyl, m-tolyl and p-tolyl, R4 is phenyl; x is 1 or 2, and y, z, p are each independently 0, 1 or 2 with the proviso that x+y+z+p=3; and mixtures thereof.
In the context of the present invention, a Lewis acid is either a single Lewis acid or else a mixture of a plurality of, for example two, three or four, Lewis acids.
Useful Lewis acids are inorganic or organic metal compounds in which the cation is selected from the group consisting of scandium, titanium, vanadium, chromium, manganese, iron, cobalt, copper, zinc, boron, aluminum, yttrium, zirconium, niobium, molybdenum, cadmium, rhenium and tin. Examples include ZnBr2, ZnI2, ZnCl2, ZnSO4, CuCl2, CuCl, Cu(O3SCF3)2, CoCl2, Col2, FeCl2, FeCl3, FeCl2, FeCl2(THF)2, TiCl4(THF)2, TiCl4, TiCl3, ClTi(O-isopropyl)3, MnCl2, ScCl3, AlCl3, Al alkyls such as Me3Al, Et3Al, Pr3Al, Bu3Al, Et2ALCN, EtAl(CN)2, (CaH17)AlCl2, (C6H17)2AlCl, (i-C4H9)2AlCl, (C5H5)2AlCl, (C6H5)AlCl2, ReCl5, ZrCl4, NbCl5, YCl3, CrCl2, MoCl5, YCl3, CdCl2, LaCl3, Er(O3SCF3)3, Yb(O2CCF3)3, SmCl3, B(C6H5)3, TaCl5, as described, for example, in U.S. Pat. No. 6,127,567, U.S. Pat. No. 6,171,996 and U.S. Pat. No. 6,380,421. Also useful are metal salts such as ZnCl2, Col2 and SnCl2, and organometallic compounds such as RAlCl2, R2AlCl, RSnO3SCF3 and R3B, where R is an alkyl or aryl group, as described, for example, in U.S. Pat. No. 3,496,217, U.S. Pat. No. 3,496,218 and U.S. Pat. No. 4,774,353.
According to U.S. Pat. No. 3,773,809, the promoter used may also be a metal in cationic form which is selected from the group consisting of zinc, cadmium, beryllium, aluminum, gallium, indium, thallium, titanium, zirconium, hafnium, erbium, germanium, tin, vanadium, niobium, scandium, chromium, molybdenum, tungsten, manganese, rhenium, palladium, thorium, iron and cobalt, preferably zinc, cadmium, titanium, tin, chromium, iron and cobalt, and the anionic moiety of the compound may be selected from the group consisting of halides such as fluoride, chloride, bromide and iodide, anions of lower fatty acids having from 2 to 7 carbon atoms, HPO32−, H3PO2−, CF3COO−, C7H15OSO2− or SO42−. Further suitable promoters disclosed by U.S. Pat. No. 3,773,809 are borohydrides, organoborohydrides and boric esters of the formula R3B and B(OR)3, where R is selected from the group consisting of hydrogen, aryl radicals having from 6 to 18 carbon atoms, aryl radicals substituted by alkyl groups having from 1 to 7 carbon atoms and aryl radicals substituted by cyano-substituted alkyl groups having from 1 to 7 carbon atoms, advantageously triphenylboron.
Moreover, as described in U.S. Pat. No. 4,874,884, it is possible to use synergistically active combinations of Lewis acids, in order to increase the activity of the catalyst system. Suitable promoters may, for example, be selected from the group consisting of CdCl2, FeCl2, ZnCl2, B(C6H5)3 and (C6H5)3SnX where X═CF3SO3, CH3C6H4SO3 or (C6H5)3BCN, and the preferred ratio specified of promoter to nickel is from about 1:16 to about 50:1.
In the context of the present invention, the term Lewis acid also includes the promoters specified in U.S. Pat. No. 3,496,217, U.S. Pat. No. 3,496,218, U.S. Pat. No. 4,774,353, U.S. Pat. No. 4,874,884, U.S. Pat. No. 6,127,567, U.S. Pat. No. 6,171,996 and U.S. Pat. No. 6,380,421.
Particularly preferred Lewis acids among those mentioned are in particular metal salts, more preferably metal halides, such as fluorides, chlorides, bromides, iodides, in particular chlorides, of which particular preference is in turn given to zinc chloride, iron(II) chloride and iron(III) chloride.
The process according to the invention is associated with a series of advantages. For instance, the hydrocyanation of 3-pentenenitrile with a low degree of conversion is possible without phase separation having to be made possible in the extractive removal of the catalyst system provided by either pre-evaporating 3-pentenenitrile or adding adiponitrile for dilution. The method of hydrocyanation with a low degree of conversion of 3-pentenenitrile which is made possible is associated with a better selectivity of adiponitrile based on 3-pentenenitrile and hydrogen cyanide. The method of hydrocyanation with a low degree of conversion of 3-pentenenitrile which is made possible is additionally associated with a higher stability of the catalyst system.
The optional treatment of the reaction effluent with ammonia or amines and the optional removal of the solids from the reaction effluent allow the process to be optimized further and the separating performance of the extraction to be adjusted.
Percentages specified hereinbelow are percent by mass based on the mixture of adiponitrile (ADN), 3-pentenenitrile (3PN) and the particular ligands. Cyclohexane was not included in the calculation.
Example 1 shows that the rate of phase separation is influenced by polar additives and the temperature.
The hydrocyanation reaction effluent used for the experiments stemed from a continuous hydrocyanation of 3-pentenenitrile (3-PN) with hydrogen cyanide to give adiponitrile (ADN) in the presence of nickel(0) complexes with chelate phosphonites of the formula A and tritolyl phosphites of the formula B
The composition of the hydrocyanation effluent obtained after removal of a portion of the unconverted pentenenitriles is reported in Table 1:
8 ml of hydrocyanation effluent are mixed intensively in a flanged bottle under argon with 2 ml of n-heptane and the amount of polar additive specified in each case in Table 2. Subsequently, the time was measured after which the n-heptane upper phase had separated from the ADN lower phase fully, partly with reformation of the rag region.
The experiments were performed with addition of acetonitrile (ACN), dimethyl sulfoxide (DMSO), dimethyleneurea (DMEU) and sulfolane at temperatures between 20 and 70° C. Table 2 summarizes the experiment results which are shown in FIG. 1.
Table 2 and FIG. 1 show that even 1% acetonitrile and, to an increased extent, 10% acetonitrile bring about a significant acceleration in phase separation between 20 and 70° C. This effect is less marked with 1% DMSO, DMEU or sulfolane. On the other hand, the phase interfaces become better visible, which likewise facilitates the phase separation.
1) % by weight of polar additive based on the mass of extractant
2) Temperature in phase separation
Example 2 shows the effects of rising amounts of acetonitrile at temperatures between 20 and 70° C.
For the experiments, the same charge of hydrocyanation effluent as in Example 1 was used. Based on 3 ml of hydrocyanation effluent, however, 6 ml of n-heptane were used. The procedure was as described in Example 1. The experiment results are compiled in Table 3 and FIG. 2.
1) % by weight of ACN based on the mass of extractant
2) Temperature in phase separation
Table 3 and FIG. 2 shows that the rate of phase separation is increased considerably with rising amount of acetonitrile and rising temperature.
Exploratory experiments showed that the addition of dimethyl sulfoxide, dimethylethyleneurea and sulfolane with increasing amount and temperature lead to a similar rise, albeit a slower rise in comparison to acetonitrile, in the rate of phase separation.
| Number | Date | Country | Kind |
|---|---|---|---|
| 06112352.7 | Apr 2006 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2007/052955 | 3/28/2007 | WO | 00 | 10/3/2008 |
