Patent Application
20200123181
A method to prepare arylalkoxysilanes involves dehydrogenative silylation between an alkoxysilane having a silicon bonded hydrogen atom and an aromatic compound having a carbon-hydrogen bond. A rhodium bisphospholane catalyst is used in the method.
Silanes having aryl groups are useful in the manufacture of polyorganosiloxane polymers for various applications, such as high temperature resins, coatings, paint additives, pump fluids, transparent encapsulants, and/or cosmetic ingredients. Current industrial methods for production of aryl functional silanes may involve a Grignard process, which generates unwanted inorganic salt by-products (such as MgCl2) and may be inefficient. Alternatively, a pseudo Friedel-Craft method may be used to prepare aryl functional silanes, however, this method may require high temperature and pressure and suffer from the further drawback of low yield. Alternatively, a direct synthesis reaction of an aryl halide with silicon metal in the presence of a copper catalyst may be used to prepare aryl functional silanes, however, this method may suffer from the drawback of generating undesirable perchlorinated biphenyl compounds. Therefore, there is an industry need for efficient methods with relatively low cost and energy to produce arylsilanes while improving yield and/or minimizing production of by-products.
A method for forming an arylalkoxysilane is disclosed herein. The method comprises:
1) combining, under conditions appropriate to form the arylalkoxysilane, starting materials comprising
A) an alkoxysilane of formula
where each R1 is independently an alkyl group of 1 to 18 carbon atoms, each R2 is independently an alkyl group of 1 to 4 carbon atoms, subscript a has an average value of at least 1, subscript b has an average value of 1 to 2, and subscript c has an average value of at least 1, and a quantity (a+b+c)=4;
B) an aromatic compound having a carbon-hydrogen bond; and
C) a rhodium bisphospholane catalyst.
In the method described above, one or more additional starting materials may be added before and/or during step 1). Optionally, D) a hydrogen acceptor and/or E) a solvent, may be added during step 1). The method described above may further comprise 2) recovering the arylalkoxysilane. Steps 1) and 2) of the method may be performed by any convenient means. For example, step 1) may be performed by heating the starting materials at a temperature from 50° C. to 150° C., alternatively 80° C. to 100° C. Step 2) may be performed by stripping and/or distillation.
Starting material A) used in the method described above is an alkoxysilane, which has at least one silicon bonded hydrogen atom per molecule. The alkoxysilane has formula
where each R1 is independently an alkyl group of 1 to 18 carbon atoms, each R2 is independently an alkyl group of 1 to 4 carbon atoms, subscript a has an average value of at least 1, subscript b has an average value of 1 to 2, and subscript c has an average value of at least 1, and a quantity (a+b+c)=4. Alkyl groups are as defined below. Alkyl groups for R1 and R2 are exemplified by methyl and ethyl. Alternatively, each R1 is methyl. Alternatively, each R2 is ethyl. Alternatively, subscript a=1, subscript b=1 or 2, and subscript c=1 or 2. Alternatively, subscript a=1, subscript b=2, and subscript c=1. Alternatively, subscript a=1, subscript b=1, and subscript c=2. Alternatively, the alkoxysilane may have formula selected from: A1)
or formula A2)
where each R1 is methyl or ethyl and each R2 is methyl or ethyl. Examples of suitable alkoxysilanes for starting material A) include dimethylethoxysilane (HMe2SiOEt); methyldiethoxysilane (HMeSi(OEt)2); or dimethylmethoxysilane (HMe2SiOMe); diethylmethoxysilane (HEt2SiOMe); or ethyldimethoxysilane (HEtSi(OMe)2).
Aromatic compounds suitable for use in the method described herein have at least one carbon-hydrogen (C—H) bond, where said carbon atom is in a ring of the aromatic compound. Suitable aromatic compounds may have an aryl group or a heteroaryl group. Suitable aromatic compounds for starting material B) include aromatic compounds comprising a 6 membered ring (e.g., 6 membered aryl ring) and aromatic compounds comprising a 5 membered ring (e.g., 5 membered heteroaryl ring). Suitable aromatic compounds comprising a 6 membered ring may have formula B1):
where each R3 is independently a hydrogen atom, a halogen atom, an alkyl group (as defined and exemplified below), a halogenated alkyl group (as defined and exemplified below), and a hydrocarbyloxy group; with the provisos that at least one R3 is hydrogen, and any two of R3, together with any atoms to which they are bonded, are optionally joined together to form a fused ring structure. Suitable halogen atoms for R3 include fluorine (F), chlorine (Cl), or bromine (Br). Suitable alkyl groups for R3 may have 1 to 4 carbon atoms (e.g., methyl or ethyl). Suitable halogenated alkyl groups for R3 may have 1 to 4 carbon atoms (e.g., CF3). Suitable hydrocarbyloxy groups R3 may be alkoxy groups of 1 to 4 carbon atoms (e.g., OCH3) or aryloxy groups of 5 to 12 carbon atoms (e.g., phenoxy). Alternatively, two of R3, together with any atoms to which they are bonded may be joined together to form a fused ring structure. Exemplary aromatic compounds of formula B1) include benzodioxole, 3-methylanisole, m-xylene, benzene, bromobenzene, chlorobenzene, fluorobenzene, and 1,3-bis(trifluoromethyl)benzene.
Suitable aromatic compounds comprising a 5 membered ring may have formula B2):
where each R4 is independently a hydrogen atom, a halogen atom, an alkyl group (as defined and exemplified below), a halogenated alkyl group (as defined and exemplified below), and a hydrocarbyloxy group; and R5 is selected from sulfur, oxygen and a nitrogen containing group of formula NR6, where each R6 is a hydrogen atom or an alkyl group of 1 to 4 carbon atoms, with the provisos that at least one R4 is hydrogen, and any two of R4, together with any atoms to which they are bonded, are optionally joined together to form a fused ring structure. Suitable halogen atoms for R4 include fluorine (F), chlorine (Cl), or bromine (Br). Suitable alkyl groups for R4 may have 1 to 4 carbon atoms (e.g., methyl or ethyl). Suitable halogenated alkyl groups for R4 may have 1 to 4 carbon atoms (e.g., CF3). Suitable hydrocarbyloxy groups R4 may be alkoxy groups of 1 to 4 carbon atoms (e.g., OCH3) or aryloxy groups of 5 to 12 carbon atoms (e.g., phenoxy). Suitable alkyl groups for R6 include methyl. Alternatively, each R5 may be the nitrogen containing group of formula NR6, where each R6 is a hydrogen atom or an alkyl group of 1 to 4 carbon atoms. Alternatively, each R5 may be an oxygen atom, with the proviso that at least one R4 is not a hydrogen atom. Alternatively, R5 may be an oxygen atom and two of R4, together with any atoms to which they are bonded, are joined together to form a fused ring structure. Exemplary aromatic compounds of formula B2) include methylfuran, benzofuran, methoxybenzofuran, furan, thiofuran, and methylpyrrole, and methylindole.
Starting materials A) and B) are combined in step 1) in relative amounts of 0.1:1 to 100:1 molar equivalents of starting material B) to starting material A) (B:A ratio). Alternatively, B:A ratio may be 1.2:1 to 10:1.
Starting material C) used in the method described herein is a rhodium bisphospholane compound. Rhodium bisphospholane compounds suitable for use as starting material C) are known in the art and are commercially available. For example, the rhodium bisphospholane compounds shown below in Table 1 are available from Aldrich.
Alternatively, method may further comprise forming the rhodium bisphospholane catalyst for starting material C) by a method comprising combining a rhodium metal precursor that does not have bisphospholane functionality and a bisphospholane compound. An organic solvent, such as tetrahydrofuran, may be added to facilitate formation of the catalyst in this method. Combining starting materials comprising the rhodium metal precursor, the bisphospholane compound and optionally the solvent may be done by any convenient means, such as mixing at room temperature or with heating to a temperature less than or equal to boiling point of the mixture prepared by mixing the starting materials. Exemplary rhodium metal precursors may have a formula selected from [Rh(R12)nR10]2 or [Rh(R12)n]+R11-; where each R12 is independently an alkene or a diene, each R10 is a negatively charged ligand, each R11 is an anion and subscript n is 1 or 2. Examples of alkenes for R12 include ethylene, cyclooctene (e.g., cis-cyclooctene) or 1-octene. Examples of dienes for R12 include 1,5-cyclooctadiene or 2,5-norbornadiene or 1,5-hexadiene. Alternatively, R12 may be selected from 1,5-cyclooctadiene and 2,5-norbornadiene. Examples of negatively charged ligands for R10 include a halogen atom such as CI or Br; a hydroxyl group; an alkoxy group of 1 to 4 carbon atoms, such as methoxy; or a hydrogen atom. Alternatively, R10 may be selected from Cl, OH, OCH3, and H. Examples of suitable anions for R11 include perchlorate, trifluoromethylsulfonate, tetrafluoroborate (BF4), tetrakisphenylborate, tetrakis(pentafluorophenyl)borate, methyltris(pentafluorophenyl)borate, tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, hexafluoroantimonate, hexafluorophosphate (PF6), [Al(C(CF3)3)4]—, carboranes such as [HCB11Me5Br6]—, (where Me represents methyl). Alternatively, the anion for R11 may be BF4 or PF6. Exemplary rhodium metal precursors are commercially available from Sigma-Aldrich Inc. or Strem Chemicals Inc., and include, for example, di-μ-chlorotetraethylene dirhodium(I); hydroxy(cyclooctadiene)rhodium(I) dimer; and rhodium bis(norbornadiene)tetrafluoroborate.
The bisphospholane compound may have formula
where R8 is a divalent hydrocarbon group and each R9 is independently a monovalent hydrocarbon group of 1 to 12 carbon atoms. The divalent hydrocarbon group for R8 is as defined below and may be an alkylene or arylene. Suitable alkylenes include ethylene. Suitable arylenes include ortho-phenylene. Suitable monovalent hydrocarbon groups for R9 include alkyl and aryl groups. Suitable alkyl groups are as defined below and include methyl, ethyl or propyl (e.g., iso-propyl). Suitable aryl groups are as defined below and include phenyl. Phospholane compounds are commercially available, for example, from Sigma-Aldrich, Inc. or Strem Chemicals. Exemplary phospholane compounds are shown in Table 2.
The rhodium metal precursor and bisphospholane compound are present in relative amounts sufficient to provide a molar ratio of bisphospholane compound: rhodium metal of 0.5:1 to 3:1, alternatively, 0.8:1 to 1.5:1.
Alternatively, the rhodium bisphospholane catalyst may have formula:
where each R8 is a divalent hydrocarbon group and each R9 is independently a monovalent hydrocarbon group of 1 to 12 carbon atoms as described above. The rhodium bisphospholane catalyst of this formula is exemplified by:
where Ph represents a phenyl group. Such a catalyst may be prepared by reacting a rhodium metal precursor, such as hydroxy(cyclooctadiene)rhodium(I) dimer and a bisphospholane compound such as (−)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane.
Alternatively, the rhodium bisphospholane catalyst may have formula:
where R8, R9, R11, R12 and subscript n are as described above.
Starting material D) a hydrogen acceptor may optionally be added during step 1) of the method described herein. Exemplary hydrogen acceptors include alkenes such as tert-butyl ethylene, heptene, or hexene; and cycloalkenes, such as cyclohexene, cycloheptene, cyclooctene, or norbornene. The hydrogen acceptor may be added in an amount of 0 to 10:1 molar equivalents of hydrogen acceptor based on the amount of starting material A) (D:A ratio). Alternatively, D:A ratio may be 1.2:1 to 2:1.
Suitable solvents include hydrocarbon solvents and/or ethers. Examples of suitable hydrocarbon solvents include hexane and/or pentane. Examples of suitable ethers include, tetrahydrofuran, 1,4-dioxane, diethylether, and/or 1,2-dimethoxyethane can be used. The amount of solvent may be 0 to 100 parts based on the weight of starting material A), alternatively 0 to 10 parts.
The method described above produces a reaction product comprising an arylalkoxysilane. The arylalkoxysilane has formula:
where R1 and R2, and subscripts b and c are as described above. Each R7 is independently an aromatic group derived from starting material B) (e.g., aryl or heteroaryl group), and subscript e≥1. Alternatively, subscript e is 1 to 2. Alternatively, subscript e=1. Alternatively, subscript e=2. In the method described above, when the aromatic compound has formula B1), then the arylalkoxysilane is exemplified by: (i) phenyldimethylethoxysilane; (ii) xylyldimethylethoxysilane; (iii) 3-methoxy-5-methylphenyl, dimethyl, ethoxysilane; (iv) phenyl, methyl, diethoxysilane; (v) fluorophenyl, dimethyl, ethoxysilane; (vi) 3,5-bis(trifluoromethyl)phenyl, dimethyl, ethoxysilane; (vii) 1,3-benzodioxole, dimethyl, ethoxysilane; (viii) chlorophenyl, dimethyl, ethoxysilane; (ix) bromophenyl, dimethyl, ethoxysilane; and (ix) phenyldimethylmethoxysilane. Alternatively, when the aromatic compound has formula B2), as described above, then the arylalkoxysilane is exemplified by: (i) 2-(ethoxydimethylsilyl)-1-methyl-1H-pyrrole; (ii) 2-(ethoxydimethylsilyl)furan; (iii) 2-(ethoxydimethylsilyl)thiophene; (iv) 1-methyl-2-(ethoxydimethylsilyl)-1H-indole; (v) 2-(ethoxydimethylsilyl)benzofuran; (vi) 5-methoxy-2-(ethoxydimethylsilyl)benzofuran; (vii) 2-(diethoxymethylsilyl)benzofuran; (viii) 2-(methoxydimethylsilyl)furan; (ix) 2-(ethoxydimethylsilyl)-5-methylfuran; (x) 2,5-bis(ethoxydimethylsilyl)furan; and (xi) 2-(diethoxymethyl)-5-methyfuran. Alternatively, the arylalkoxysilane may be selected from the group consisting of: 2-(ethoxydimethylsilyl)-1-methyl-1H-pyrrole and 1-methyl-2-(ethoxydimethylsilyl)-1H-indole. Alternatively, the arylalkoxysilane may be selected from the group consisting of 2-(ethoxydimethylsilyl)benzofuran; 5-methoxy-2-(ethoxydimethylsilyl)benzofuran; 2-(diethoxymethylsilyl)benzofuran; 2-(ethoxydimethylsilyl)-5-methylfuran; 2,5-bis(ethoxydimethylsilyl)furan; and 2-(diethoxymethyl)-5-methyfuran.
Alternatively, in the arylalkoxysilane of formula:
each R1 is independently an alkyl group of 1 to 18 carbon atoms, each R2 is independently an alkyl group of 1 to 4 carbon atoms, subscript b has an average value of 1 to 2, subscript c has an average value of at least 1, with the proviso that a quantity (b+c)=3; subscript e≥1, and each R7 is a pyrrolyl or indolyl group. Alternatively, each R1 has 1 to 12 carbon atoms, alternatively 1 to 6 carbon atoms, alternatively 1 to 4 carbon atoms; and alternatively each R1 is methyl or ethyl. Alternatively, each R2 has 1 to 12 carbon atoms, alternatively 1 to 6 carbon atoms, alternatively 1 to 4 carbon atoms; and alternatively each R2 is methyl or ethyl. Alternatively, each R7 is a 1-methyl-1H-pyrrole group or 1-methyl-1H-indole group. Arylalkoxysilanes of this formula include 2-(ethoxydimethylsilyl)-1-methyl-1H-pyrrole and 1-methyl-2-(ethoxydimethylsilyl)-1H-indole.
Alternatively, in the arylalkoxysilane of formula:
each R1 is independently an alkyl group of 1 to 18 carbon atoms, each R2 is independently an alkyl group of 1 to 4 carbon atoms, subscript b has an average value of 1 to 2, subscript c has an average value of at least 1, with the proviso that a quantity (b+c)=3; subscript e≥1, and each R7 is a substituted furyl group, i.e., a furyl group wherein one carbon atom is bonded to the silicon atom shown in the formula above and at least one other carbon atom in the ring is bonded to a substituent other than hydrogen, i.e., in the aromatic compound of formula B2) above, at least one R4 is not a hydrogen atom and/or two of R4, together with any atoms to which they are bonded, are joined together to form a fused ring structure. Alternatively, in this formula R7 is selected from the group consisting of benzofuran, 5-methyl furan, and 5-methoxy benzofuran. In this embodiment, the arylalkoxysilane is exemplified by 2-(ethoxydimethylsilyl)benzofuran; 5-methoxy-2-(ethoxydimethylsilyl)benzofuran; 2-(diethoxymethylsilyl)benzofuran; 2-(ethoxydimethylsilyl)-5-methylfuran; 2,5-bis(ethoxydimethylsilyl)furan; and 2-(diethoxymethyl)-5-methyfuran.
These examples are intended to illustrate some embodiments of the invention and should not be interpreted as limiting the scope of the invention set forth in the claims. All air-sensitive materials were handled under an argon or nitrogen atmosphere. THF was dried with two successive activated alumina columns and stored under molecular sieves. Other commercially available chemicals were used as received. Conversion was calculated based on NMR analysis or GC-Ms analysis.
[(Ph-BPE)Rh(μ-Cl)]2 was prepared according to this Reference Example 1. To a solution of [Rh(ethylene)2Cl]2 (156 mg, 0.4 mmol) in THF, (−)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane ((R,R)-Ph-BPE) in THF (400 mg, 0.79 mol) was slowly added. After stirring at room temperature for 3 hours, the filtration of the reaction mixture gave a deep orange solution. Removal of volatiles under vacuum followed by trituration with hexanes gave yellowish orange solids. Recrystallization of products by layering hexanes onto benzene solution afforded [(Ph-BPE)Rh(μ-Cl)]2 as orange crystals.
1H NMR (400 MHz, CDCl3): δ 7.98 (d, 8H, J=7.4 Hz), 7.43 (t, 8H, J=6.8 Hz), 7.35-7.31 (m, 4H), 7.16-7.01 (m, 20H), 4.41-3.35 (m, 4H), 2.59-2.52 (m, 4H), 2.46-2.36 (m, 4H), 2.03-1.84 (m, 8H), 1.63-1.53 (m, 4H), 0.50-0.26 (m, 8H). 31P NMR (CDCl3): δ 106.0, 104.8.
[(Ph-BPE)Rh(μ-H)(μ-Cl)Rh(Ph-BPE)] was prepared according to this Reference Example 2. To a benzene solution (10 ml) of the [(Ph-BPE)Rh(μ-Cl)]2 prepared in Reference Example 1 (260 mg, 0.2 mmol), HMe2Si(OEt) (2.8 ml) was added. After stirring at 100° C. for 10 hours, volatiles were removed under vacuum. Recrystallization of products by layering hexanes onto benzene solution afforded [(Ph-BPE)Rh(μ-H)(μ-CI)Rh(Ph-BPE)] as orange crystals.
1H NMR (400 MHz, CDCl3): δ 8.02 (d, 8.0 Hz, 4H, Ph), 7.93 (d, 8.0 Hz, 4H, Ph), 7.51 (t, 7.6 Hz, 4H, Ph), 7.37 (t, 7.4 Hz, 2H, Ph), 6.95-7.23 (m, 22H, Ph), 6.93 (t, 7.4 Hz, 4H, Ph), 4.57 (m, 2H), 4.06 (m, 2H), 2.81 (m, 2H), 2.64 (m, 2H), 2.49 (m, 2H), 2.35 (m, 2H), 1.85-2.14 (m, 8H), 1.71 (br q, 4H), 0.80-0.95 (br m, 4H), 0.01 (m, 4H), −7.91 (br m, 1H, RhH). 31P NMR (161.84 MHz, CDCl3): δ 103.8 (m), 102.6 (m), 99.9 (m), 98.8 (m).
In this example 1, phenyldimethylethoxysilane
was prepared as follows. An oven-dried vial was charged with [(Ph-BPE)Rh(μ-Cl)]2 (6.5 mg, 0.5 mol %), benzene (1 mL), and cyclohexene (99 mg, 1.2 equiv.). After stirring for 1 h at 100° C., the reaction mixture was cooled to RT. To the mixture, HSiMe2(OEt) (104 mg, 1 mmol) was added. The reaction mixture was allowed to stir for 20 hours at 100° C. (>98% conversion, 94% yield by 1H NMR). The resulting mixture was concentrated and purified by silica gel chromatography affording the desired product PhMe2Si(OEt) as a colorless liquid (88 mg, 49% yield). Note that the product is decomposed on silica gel. For arenes which have low boiling point (<110° C.), clean product can be obtained after following workup procedure: the evaporation of the crude mixture, dissolving the residue in hexane, filtration through a plug of Celite, and concentration of filtrate. 1H NMR (400 MHz, CDCl3): δ 7.61-7.58 (m, 2H), 7.41-7.35 (m, 3H), 3.68 (q, 2H, J=7.0 Hz), 1.19 (t, 3H, J=7.0 Hz), 0.39 (s, 6H) 29Si NMR (79.4 MHz, CDCl3): δ 7.0
In this comparative example 1, Rh/Bis(biarylphosphine)-catalyzed C—H silylation with HSiMe2(OEt) was performed. An oven-dried vial was charged with [Rh(cod)OH]2 (2.3 mg, 0.005 mol), (R)-(+)-2,2′-Bis[di(3,4,5-trimethoxyphenyl)phenyl]phosphino]-6,6′-dimethoxy-1,1′-biphenyl with formula
(12.7 mg, 0.011 mmol) and benzene (1 mL). To the mixture, HSiMe2(OEt) (104 mg, 1 mmol) and cyclohexene (99 mg, 1.2 equiv.) were added. The reaction mixture was allowed to stir for 20 hours at 80° C. and the crude product mixture was analyzed PhMe2Si(OEt): <1% yield by GC-Ms).
In this example 2, phenyldimethylethoxysilane, PhMe2Si(OEt), was prepared as follows. In an oven-dried vial, [Rh(cod)(OH)]2 (4.6 mg, 0.01 mmol) and (S,S)-i-Pr-BPE (7.4 mg, 0.02 mmol) were placed. Benzene (1 ml), HMe2Si(OEt) (104 mg, 1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 24 hours at 80° C. GC-Ms analysis shows HMe2Si(OEt) disappeared completely. 1H NMR and GC-Ms analysis confirms formation of PhMe2Si(OEt) (GC-Ms yield: 85%). This example demonstrates that a catalyst may be formed in situ by reaction of a rhodium precursor with a bisphospholane ligand.
In this example 3, a xylyldimethylethoxysilane of formula
was prepared as follows. In an oven-dried vial, [Rh(cod)(OH)]2 (4.6 mg, 0.01 mmol) and (S,S)-i-Pr-BPE (7.4 mg, 0.02 mmol) were placed. m-Xylene (1 ml), HMe2Si(OEt) (104 mg, 1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 24 hours at 80° C. (GC-Ms yield: 38%). The resulting mixture was concentrated and purified by silica gel chromatography affording the desired product as a colorless liquid. 29Si NMR (79.4 MHz, CDCl3): δ 7.2 (s)1H NMR (400 MHz, CDCl3): δ 7.19 (br, 2H, xylyl), 7.04 (br, 1H, xylyl), 3.68 (q, 6.9 Hz, 2H, OCH2CH3), 2.33 (s, CH3-Ph), 1.19 (t, 7.0 Hz, 3H, OCH2CH3), 0.36 (s, 6H, CH3Si).
In this example 4, 3-methoxy-5-methylphenyl, dimethyl, ethoxysilane of formula
was prepared as follows. In an oven-dried vial, a mixture of [Rh(cod)(OH)]2 (4.6 mg, 0.01 mmol) and (S,S)-i-Pr-BPE (7.4 mg, 0.02 mmol) was prepared. 3-methylanisole (1 ml), HMe2Si(OEt) (1 mmol, 0.14 ml) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 24 hours at 80° C. GC-Ms analysis confirms formation of (3-methoxy-5-methylphenyl)Me2Si(OEt) (GC-Ms yield: 67%).
In this example 5, phenyl, methyl, diethoxysilane of formula
was prepared as follows. In an oven-dried vial, [Rh(cod)(OH)]2 (4.6 mg, 0.01 mmol) and (S,S)-i-Pr-BPE (7.4 mg, 0.02 mmol) were placed. Benzene (1 ml), HMeSi(OEt)2 (134 mg, 1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 24 hours at 80° C. GC-Ms analysis confirms formation of PhMeSi(OEt)2 (GC-Ms yield: 20%).
Examples 6 to 20 were conducted using the following procedure. An oven-dried vial was charged with [(Ph-BPE)Rh(μ-Cl)]2 (6.5 mg, 0.5 mol %), an aromatic compound (0.5 mL or 1 mL), and cyclohexene (99 mg, 1.2 equiv.). After stirring for 1 h at 100° C., the reaction mixture was cooled to RT. To the mixture, an amount of an alkoxysilane was added. The reaction mixture was allowed to stir for 20 h at 100° C. The resulting product was evaluated by 1H NMR. The aromatic compound used and whether cyclohexene was added are shown below in Table 4. The 1H NMR results are shown in Table 5.
In this example 21, a 2-(ethoxydimethylsilyl)-5-methylfuran of formula
was prepared as follows. In an oven-dried vial, [(Ph-BPE)Rh(μ-H)(μ-Cl)Rh(Ph-BPE)] (6.3 mg, 0.5 mol %) was placed. 2-methylfuran (1 ml), HMe2Si(OEt) (0.14 ml, 1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 20 hours at 80° C. 1H NMR analysis confirms formation of the target compound (NMR yield: 95%). 1H NMR (400 MHz, CDCl3): δ 6.63 (m, 1H, furyl), 5.98 (m, 1H, furyl), 3.70 (q, 7.1 Hz, 2H, OCH2CH3), 2.33 (dd, 3H, CH3-furyl), 1.18 (t, 7.0 Hz, 3H, OCH2CH3), 0.36 (s, 6H, Si(CH3)2)29Si NMR (79.4 MHz, CDCl3): δ −2.4 (s)
In this example 22, a 2,5-bis(ethoxydimethylsilyl)furan of formula
was prepared as follows. In an oven-dried vial, [(Ph-BPE)Rh(μ-H)(μ-Cl)Rh(Ph-BPE)] (6.3 mg, 0.5 mol %) was placed. Furan (1 ml), HMe2Si(OEt) (1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 20 hours at 80° C. Volatiles were removed under vacuum. To the product mixture, HMe2Si(OEt) (1 mmol), THF (0.1 ml) and cyclohexene (1.1 mmol) were added and stirred for 20 hrs at 80° C. Removal of volatiles afforded yellow liquid. 1H NMR (400 MHz, CDCl3): δ 6.73 (s, 2H, furyl), 3.70 (q, 6.9 Hz, 4H, OCH2CH3), 1.16 (t, 7.0 Hz, 6H, OCH2CH3), 0.38 (s, 12H, SiCH3) 13C NMR (100 MHz, CDCl3): δ 162.9 (s), 120.5 (s), 59.1 (s), −1.84 (s)29Si NMR (79.4 MHz, CDCl3): δ −1.8 (s)
In this example 23, a 2-(diethoxymethyl)-5-methylfuran of formula
was prepared as follows. In an oven-dried vial, [(Ph-BPE)Rh(μ-H)(μ-Cl)Rh(Ph-BPE)] (6.3 mg, 0.5 mol %) was placed. 2-methylfuran (1 ml), HMeSi(OEt)2 (134 mg, 1 mmol) and cyclohexene (1.1 mmol) were added to the vial. The reaction mixture was allowed to stir for 20 hours at 100° C. 1H NMR analysis confirms formation of the target compound (NMR yield: 93%). 1H NMR (400 MHz, CDCl3): δ 6.71 (dq, 2.8 Hz and 0.4 Hz, 1H, furyl), 5.98 (dq, 3.2 Hz and 1.1 Hz, 1H, furyl), 3.84 (q, 7.1 Hz, 4H, OCH2CH3), 2.33 (m, 3H, CH3-furyl), 1.24 (t, 7.0 Hz, 6H, OCH2CH3), 0.34 (s, 3H, SiCH3)13C NMR (100 MHz, CDCl3): δ 157.3 (s), 123.4 (s), 59.1 (s), 105.8 (s), 59.0 (s), 18.4 (s), 13.9 (s), −3.8 (s)29Si NMR (79.4 MHz, CDCl3): δ −26.3 (s)
In this example 24, phenyl, dimethyl, ethoxysilane of formula
was prepared as follows. An oven-dried vial was charged with [Rh(nbd)2BF4] (7.5 mg, 2 mol %), (S,S)-Ph-BPE (11 mg, 2.2 mol %), benzene (1 mL), and cyclohexene (99 mg, 1.2 equiv.). After stirring for 1 h at 100° C., the reaction mixture was cooled to RT. To the mixture, HSiMe2(OEt) (104 mg, 1 mmol) was added. The reaction mixture was allowed to stir for 20 hours at 100° C. (27% yield by 1H NMR).
In this example 25, phenyl, dimethyl, ethoxysilane of formula
was prepared as follows. An oven-dried vial was charged with [Rh(i-Pr-DuPhos)cod]BF4 (14 mg, 2 mol %), benzene (1 mL), and cyclohexene (99 mg, 1.2 equiv.). After stirring for 1 h at 80° C., the reaction mixture was cooled to RT. To the mixture, HSiMe2(OEt) (104 mg, 1 mmol) was added. The reaction mixture was allowed to stir for 20 hours at 80° C. (9% yield by 1H NMR).
The examples above show that the dehydrogenative silylation method described herein can be used to produce various arylalkoxysilanes. The rhodium bisphospholane catalyst may provide the benefit of allowing an alkoxysilane having a silicon bonded hydrogen atom to be used as a starting material to prepare the arylalkoxysilanes. Because the starting material and product contain at least one alkoxy group bonded to silicon, the arylalkoxysilane produced by the method is reactive with, e.g., polyorganosiloxanes having silicon bonded hydrogen atoms or silicon bonded hydrolyzable groups. The arylalkoxysilanes produced by the method described herein may be useful as endblockers for such polyorganosiloxanes.
All amounts, ratios, and percentages are by weight unless otherwise indicated. The articles ‘a’, ‘an’, and ‘the’ each refer to one or more, unless otherwise indicated. The disclosure of ranges includes the range itself and also anything subsumed therein, as well as endpoints. For example, disclosure of a range of 2.0 to 4.0 includes not only the range of 2.0 to 4.0, but also 2.1, 2.3, 3.4, 3.5, and 4.0 individually, as well as any other number subsumed in the range. Furthermore, disclosure of a range of, for example, 2.0 to 4.0 includes the subsets of, for example, 2.1 to 3.5, 2.3 to 3.4, 2.6 to 3.7, and 3.8 to 4.0, as well as any other subset subsumed in the range. Similarly, the disclosure of Markush groups includes the entire group and also any individual members and subgroups subsumed therein. For example, disclosure of the Markush group a hydrogen atom, an alkyl group, an alkenyl group, or an aryl group, includes the member alkyl individually; the subgroup alkyl and aryl; and any other individual member and subgroup subsumed therein.
“Alkyl” means a saturated monovalent hydrocarbon group. Alkyl is exemplified by, but not limited to, methyl, ethyl, propyl (e.g., iso-propyl and/or n-propyl), butyl (e.g., isobutyl, n-butyl, tert-butyl, and/or sec-butyl), pentyl (e.g., isopentyl, neopentyl, and/or tert-pentyl); hexyl, heptyl, octyl, nonyl, and decyl, as well as branched saturated monovalent hydrocarbon groups of 6 or more carbon atoms.
“Alkenyl” means a monovalent hydrocarbon group containing a double bond. Alkenyl groups are exemplified by, but not limited to, ethenyl, propenyl (e.g., iso-propenyl and/or n-propenyl), butenyl (e.g., isobutenyl, n-butenyl, tert-butenyl, and/or sec-butenyl), pentenyl (e.g., isopentenyl, n-pentenyl, and/or tert-pentenyl), hexenyl, heptenyl, octenyl, nonenyl, and decenyl, as well as such branched groups of 6 or more carbon atoms.
“Alkynyl” means a monovalent hydrocarbon group containing a triple bond. Alkynyl groups are exemplified by, but not limited to, ethynyl, propynyl (e.g., iso-propynyl and/or n-propynyl), butynyl (e.g., isobutynyl, n-butynyl, tert-butynyl, and/or sec-butynyl), pentynyl (e.g., isopentynyl, n-pentynyl, and/or tert-pentynyl), hexynyl, heptynyl, octynyl, nonynyl, and decynyl, as well as such branched groups of 6 or more carbon atoms.
“Aryl” means a cyclic, fully unsaturated, hydrocarbon group. Aryl is exemplified by, but not limited to, cyclopentadienyl, phenyl, anthracenyl, and naphthyl. Monocyclic aryl groups may have 5 to 9 carbon atoms, alternatively 6 to 7 carbon atoms, and alternatively 5 to 6 carbon atoms. Polycyclic aryl groups may have 10 to 18 carbon atoms, alternatively 10 to 14 carbon atoms, and alternatively 12 to 14 carbon atoms.
“Aralkyl” means an alkyl group having a pendant and/or terminal aryl group or an aryl group having a pendant alkyl group. Exemplary aralkyl groups include tolyl, xylyl, benzyl, phenylethyl, phenyl propyl, and phenyl butyl.
“Carbocycle” and “carbocyclic” each mean a hydrocarbon ring. Carbocycles may be monocyclic or alternatively may be fused, bridged, or spiro polycyclic rings. Monocyclic carbocycles may have 3 to 9 carbon atoms, alternatively 4 to 7 carbon atoms, and alternatively 5 to 6 carbon atoms. Polycyclic carbocycles may have 7 to 18 carbon atoms, alternatively 7 to 14 carbon atoms, and alternatively 9 to 10 carbon atoms. Carbocycles may be saturated or partially unsaturated.
“Cycloalkyl” means saturated carbocycle. Monocyclic cycloalkyl groups are exemplified by cyclobutyl, cyclopentyl, and cyclohexyl.
Collectively, the term “monovalent hydrocarbon group” includes alkyl, alkenyl, aryl, aralkyl, and carbocyclic groups, as defined above.
“Divalent hydrocarbon group” includes alkylene groups such as ethylene, propylene (including isopropylene and n-propylene), and butylene (including n-butylene, t-butylene and isobutylene); and pentylene, hexylene, heptylene, octylene, and branched and linear isomers thereof; arylene groups such as phenylene, e.g., ortho-phenylene; and alkaralkylene groups such as:
Alternatively, each divalent hydrocarbon group may be ethylene, propylene, butylene or hexylene. Alternatively, each divalent hydrocarbon group may be ethylene or propylene.
“Halogenated hydrocarbon” means a hydrocarbon group as defined above, but where one or more hydrogen atoms bonded to a carbon atom have been formally replaced with a halogen atom. For example, monovalent halogenated hydrocarbon groups can be any one of alkyl, alkenyl, aryl, aralkyl, and carbocyclic groups in which one or more hydrogen atoms bonded to a carbon atom have been replaced with a halogen atom. Monovalent halogenated hydrocarbon groups include halogenated alkyl groups, halogenated carbocyclic groups, and halogenated alkenyl groups. Halogenated alkyl groups include fluorinated alkyl groups such as trifluoromethyl (CF3), fluoromethyl, trifluoroethyl, 2-fluoropropyl, 3,3,3-trifluoropropyl, 4,4,4-trifluorobutyl, 4,4,4,3,3-pentafluorobutyl, 5,5,5,4,4,3,3-heptafluoropentyl, 6,6,6,5,5,4,4,3,3-nonafluorohexyl, and 8,8,8,7,7-pentafluorooctyl; and chlorinated alkyl groups such as chloromethyl and 3-chloropropyl. Halogenated carbocyclic groups include fluorinated cycloalkyl groups such as 2,2-difluorocyclopropyl, 2,3-difluorocyclobutyl, 3,4-difluorocyclohexyl, and 3,4-difluoro-5-methylcycloheptyl; and chlorinated cycloalkyl groups such as 2,2-dichlorocyclopropyl, 2,3-dichlorocyclopentyl. Halogenated alkenyl groups include chloro allyl.
“Heterocycle” and “heterocyclic” refer to a ring group comprised of carbon atoms and one or more heteroatoms in the ring. The heteroatom may be N, O, P, S, or a combination thereof. Heterocycles may be monocyclic or alternatively may be fused, bridged, or spiro polycyclic rings. Monocyclic heterocycles may have 3 to 9 member atoms in the ring, alternatively 4 to 7 member atoms, and alternatively 5 to 6 member atoms. Polycyclic heterocycles may have 7 to 17 member atoms, alternatively 7 to 14 member atoms, and alternatively 9 to 10 member atoms. Heterocycles may be saturated or partially unsaturated. A “heteroaryl group” is a fully unsaturated ring group comprised of carbon atoms and one or more heteroatoms in the ring.
“Aromatic compound” refers to a compound having an aryl group and/or a compound having a heteroaryl group.
This application claims the benefit under 35 U.S.C. § 119 (e) of U.S. Provisional Application Ser. No. 62/484,030 filed on 11 Apr. 2017. U.S. Provisional Application Ser. No. 62/484,030 is hereby incorporated by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2018/023915 | 3/23/2018 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62484030 | Apr 2017 | US |
