Patent Grant
8791305
The present invention relates to novel ligands and catalyst systems for hydroformylation processes of short and long chain olefins, for example for the hydroformylation of allyl alcohol to produce 4-hydroxybutyraldehyde. The preparation of these ligands and catalysts as well as their use in hydroformylation reactions is disclosed.
The hydroformylation of allyl alcohol is known and is utilized industrially (see e.g. U.S. Pat. No. 4,064,145; U.S. Pat. No. 4,215,077; U.S. Pat. No. 4,238,419; U.S. Pat. No. 4,678,857; U.S. Pat. No. 5,290,743). Allyl alcohol is reacted in these processes with CO/H2 gas mixtures, giving 4-hydroxybutyraldehyde (HBA). Following distillative removal of undesired by-products, HBA is hydrogenated in a known manner to give 1,4-butanediol (BDO).
Recently, rhodium complexes together with diphosphine ligands such as DIOP (2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis-[bis(3,5-dimethylphenyl)phosphino]-butane) have been employed for hydroformylation reactions.
A general disadvantage of this mode of production is the formation of undesired by-products. In particular, as well as the desired linear product, the isomeric branched product 3-hydroxy-2-methylpropionaldehyde (HMPA) and other C3 by-products such as n-propanol and propionaldehyde are formed. This adversely affects the economic viability of the process.
The present invention provides phosphine ligands which are based on a cyclobutane ligand containing at least two trans-coordinated (3,5-dialkyl-phenyl)phosphinomethyl groups. In a further aspect, the present invention provides catalyst systems which are formed from a rhodium complex and said cyclobutane ligand comprising at least two trans-coordinated (3,5-dialkylphenyl)-phosphinomethyl groups.
The ligands and catalyst systems of the present invention allow more favorable HBA:HMPA-proportions to be achieved in the hydroformylation of allyl alcohole, and thus provide improved selectivity and high reaction yields.
Generally, the phosphine ligands disclosed in this invention can be defined as phosphinomethyl-cyclobutanes having the formula [A]
wherein
R1 is alkyl, preferably methyl, ethyl or propyl
R2 is H or an alkoxy group,
R3 and R4, independently of one another, are CH2OR1, CH2O-aralkyl, CH2OH, CH2—[P(3,5-R1,R1-4-R2-phenyl)2] or CH2O—(CH2—CH2—O)m—H (with m being an integer between 1 and 1,000)
Preferably, [A] is an all-trans-phosphinomethyl-cyclobutane derivative and the phosphine ligands are all-trans-phosphinomethyl-cyclobutanes of formula [A],
wherein
R1 is methyl, ethyl or propyl,
R2 is H,
R3 and R4, independently of one another, are CH2OR1, CH2OH or CH2—[P(3,5-R1,R1-4-R2-phenyl)2]
Further preferred are the ligands [A] having the composition
In a still further preferred embodiment, the phosphine ligands are all-trans-phosphinomethyl-cyclobutanes of formula [A], wherein
R1 is methyl, ethyl or propyl,
R2 is H,
R3 and R4 are CH2—[P(3,5-R1,R1-4-R2-phenyl)2].
In addition to the phosphine ligands of formula [A], the catalysts and catalyst systems of the present invention also comprise a rhodium complex. Examples for suitable rhodium complexes include (acetylacetonato)-dicarbonyl-rhodium(I) [Rh(CO)2acac], tris-(triphenylphosphine)-rhodium-carbonyl-hydride[Rh(PPh)3(CO)H], (triphenylphosphine)-carbonyl-rhodium(I)-acetylacetonate[Rh(CO)(PPh3)acac], cyclooctadienylrhodium(I)-chloride-dimer[(COD)RhCl]2 and Rh(III)-ethylhexanoate. The preferred Rh complex is (acetylacetonato)-dicarbonyl-rhodium(I).
In the practice of this invention, the rhodium complex is employed in such an amount that the Rh concentration within the reaction mixture ranges from about 0.05 to 100 mg Rh/l, preferably 0.1 to 25 mg Rh/l. Lower Rh concentrations may reduce the reaction rate and yield.
The molar ratio of the phosphinomethyl-cyclobutane ligand:rhodium complex is generally in the range of 0.5:1 to 10:1, preferably in the range of 1:1 to 5:1. Usually, the phosphinomethyl-cyclobutane ligand and the rhodium complex are added to the reaction mixture before the olefine compound (e.g. allyl alcohol) is added.
Usually, the hydroformylation of olefinic compounds such as allyl alcohol is carried out in homogeneous phase. Polar and/or non-polar solvents may be employed. Polar solvents which may be used are, for example, ethanol, n-propanol, iso-propanol n-butanol, isobutanol. Suitable non-polar solvents are aromatic or aliphatic hydrocarbons, such as benzene, toluene or xylene. Generally, the solvents used in the process should be able to solubilize the rhodium complex employed.
Basically, the ligands and catalyst systems of the present invention can be used in hydroformylation reactions of short and long-chain olefins. As examples for short-chain olefins, there may be mentioned ethylene, propylene, 1-butene, isobutene, 1-pentene and the like.
Preferably, the ligands and catalyst systems of the present invention are employed in the hydroformylation of allylalcohol. In this specific application, the ligands and catalyst systems allow more favorable HBA:HMPA-proportions to be achieved, and thus provide improved selectivity and high reaction yields.
An additional aspect of the invention is the use of the catalyst systems containing the ligands of the formula [A] which permit different embodiments of the hydroformylation process.
Novel hydrophilic catalyst systems comprising the ligands of the formula [A] with polyether groups (such as CH2O—(CH2—CH2—O)m—H with m being an integer between 1 and 1,000) may be used in membrane reactors and thus allow the process products to be separated off continuously after the hydroformylation.
The hydroformylation takes place under reaction conditions known in the prior art, typically in a temperature range from 20 to 120° C. and in a pressure range from 2-20 bar. The optimum performance is ascertained by appropriate preliminary experiments depending on the existing equipment.
The molar ratio of the synthesis gas mixture (CO/hydrogen) employed is CO:H2˜1:1, but it can vary considerably depending on the embodiment.
The reaction time is in the range of 0.5 to 4 hours. At the start of the reaction, the allyl alcohol concentration is 5 to 50%, preferably 10 to 25%, based on the solvent or solvent mixture.
After the reaction, HBA, HMPA and other by-products are separated off from the catalyst, preferably by extraction with water.
In a later step, HBA (and HMPA) are hydrogenated to give the corresponding dihydroxy compounds, and fractional distillation of the crude product gives the desired 1,4-butanediol (BDO) in pure form.
The examples below further illustrate the invention:
88 mg (0.5 mmol) of all-trans-1,2,3,4-tetra(hydroxymethyl)cyclobutane were dissolved in 3 ml of anhydrous pyridine and, at 0° C., 251 mg (0.9 mmol) of trityl chloride were added with intense stirring. The reaction mixture was kept at 0° C. overnight with stirring. Then, it was added to 10 ml of water and extracted with ethyl acetate (3×5 ml), then dried with MgSO4 and evaporated to dryness in a rotary evaporator.
The crude product was separated off by chromatography (silica gel). (Eluent:ethyl acetate:hexane 1:3→2:3→ethyl acetate:methanol 95:5).
The main product obtained was 114 mg (34% of theory) of all-trans-1,2-bis(hydroxymethyl)-3,4-bis(trityloxymethyl)cyclobutane.
In a manner known in the art, the two OH-groups of this compound are tosylated and reacted with LiP(3,5-xylyl)2 to yield all-trans-1,2-bis[bis-(3,5-xylyl)phosphinomethyl]-3,4-bis(trityloxymethyl)-cyclobutane. In further steps (optional), the two trityl groups may be removed or may be exchanged by alkyl or alkoxy groups.
The starting compound all-trans-1,2,3,4-tetra(hydroxymethyl)-cyclobutane is tosylated in a matter known per se by reaction with 4 equivalents of tosylchloride (p-toluolsulfonic acid chloride) in the presence of a base in a chlorinated hydrocarbon solvent (e.g. dichloromethane) in the presence of a base (e. pyridine). The tetra-tosylated compound is isolated and the solvent is removed in vacuo.
In the next step, the tetra-tosylated compound is reacted with 4 equivalents of LiP(3,5-xylyl)2 in a dry ether solvent (e.g. EG/DME mixture) to yield the all-trans tetraphosphinomethyl-cyclobutane ligand.
In 4 ml of dried and degassed tert-butyl methyl ether, 16 mmol of all-trans-1,2,3,4-tetra[bis-(3,5-xylyl)phosphinomethyl]-cyclobutane are reacted under argon with [Rh(CO)2(acac)](8 mmol).
The resulting solution is injected into an autoclave under argon and flushed with a CO:H2-1:1 mixture. Via a side arm, a solution of 1 ml of allyl alcohol in 15 ml of ethanol is then added and the reaction is carried out at a pressure of 40 bar and a temperature of 120° C. This gives 97% of theory of HBA+HMPA in a ratio of ca. 14:1 (selectivity HBA/HMPA=93.3%).
These experiments are conducted in a 60 ml autoclave under argon at a temperature of 65° C. and a pressure of p=20 bar of synthesis gas (CO/H2=1:1). The reaction time is 120 mins.
A solution of the respective phosphine ligand (2 equivalents or 8.6×10−5 mole) in 15 grams of dry degassed toluene is added to [Rh(CO)2acac] (1 equivalent or 4.3×10−5 mole) in the autoclave. The autoclave is pressurized at 20 bar, then heated to 65° C. and the allyl alcohol (3.5 ml) is injected. After 120 mins, the gas uptake is completed and the autoclave is cooled. The resulting solution is analyzed by gas chromatography to determine the reaction products 4-hydroxyl-butyraldehyde (HBA) and 3-hydroxy-2-methylpropionaldehyde (HMPA). The selectivity is determined by the ratio of the product peak area (HBA) vs. the side product peak area (HMPA). The results are summarized in Table 1:
As can be seen from Table 1, the ligands and catalytic systems of the present invention allow more favorable HBA:HMPA-proportions to be achieved in the hydroformylation of allyl alcohole, and thus provide improved selectivity and high reaction yields.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2011 102 666 | May 2011 | DE | national |
| 10 2011 110 621 | Aug 2011 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2012/059850 | 5/25/2012 | WO | 00 | 1/3/2014 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2012/163837 | 12/6/2012 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4064145 | Taylor | Dec 1977 | A |
| 4215077 | Matsumoto et al. | Jul 1980 | A |
| 4238419 | Matsumoto et al. | Dec 1980 | A |
| 4678857 | Dureanleau et al. | Jul 1987 | A |
| 5290743 | Chang | Mar 1994 | A |
| 7279606 | White | Oct 2007 | B1 |
| 7294602 | White | Nov 2007 | B1 |
| 7655821 | White et al. | Feb 2010 | B1 |
| Number | Date | Country |
|---|---|---|
| 2008121194 | Oct 2008 | WO |
| 2010132087 | Nov 2010 | WO |
| 2012163831 | Dec 2012 | WO |
| Entry |
|---|
| Boogaerts, et al. (2010) “High chemo and regioselective formation of alcohols from the hydrocarbonylation of alkenes using cooperative ligand effects” Chem. Commun., 46, 2194-2196. |
| International Search Report for Application No. PCT/EP2012/059850 mailed Aug. 3, 2012 (in English). |
| Number | Date | Country | |
|---|---|---|---|
| 20140114090 A1 | Apr 2014 | US |
