Process for making haloorganoalkoxysilanes
View Patent ↗A haloorganoalkoxysilane is prepared by reacting an olefinic halide with an alkoxysilane in which the alkoxy group(s) contain at least two carbon atoms in a reaction medium to which has been added a catalytically effective amount of ruthenium-containing catalyst and a reaction-promoting effective amount of an electron-donating aromatic compound promoter. The process can be used to prepare, inter alia, chloropropyltriethoxysilane, which is a key intermediate in the manufacture of silane coupling agents.
1. A process for preparing a haloorganoalkoxysilane of the formula
(R 1 ) x (R 2 O) 3-x SiCH 2 CHR 3 CR 4 R 5 X
wherein R 1 in an alkyl of from 1 to 6 carbon atoms, R 2 is an alkyl of from 1 to 6 carbon atoms, R 3 is an alkyl group of 1 to 6 carbon atoms or hydrogen, R 4 is an alkyl of from 1 to 6 carbon atoms, hydrogen or halogen, R 5 is hydrogen or an alkyl of from 1 to 6 carbon atoms, X is a halogen, x is 0, 1 or 2, which comprises reacting an olefinic halide of the general formula:
H 2 C═CR 3 CR 4 R 5 X
wherein R 3 , R 4 , R 5 and X have the aforestated meanings, with a molar excess of alkoxysilane of the general formula:
(R 1 ) x (R 2 O) 3-x SiH
wherein R 1 and R 2 and x have the aforestated meanings, in a reaction medium to which has been added a catalytically effective amount of ruthenium-containing catalyst and an electron-donating aromatic compound in an amount of about 1 to about 100 mole equivalents versus the moles of ruthenium metal; wherein the yield of the haloorganoalkoxysilane exceeds 87 mole percent, based upon the total reaction products.
2. The process of claim 1 , wherein the olefinic halide is selected from the group consisting of allyl chloride, methallyl chloride, 3-chloro-1-butene, 3, 4-dichloro-1-butene and 2-chloropropene.
3. The process of claim 1 , wherein the alkoxysilane is selected from the group consisting of trimethoxysilane, methyldimethoxysilane, dimethylmethoxysilane, triethoxysilane methyldiethoxysilane, dimethylethoxysilane, ethyldiethoxysilane, and diethylethoxysilane.
4. The process of claim 1 , wherein the olefinic halide is allyl chloride and the alkoxysilane in diethylethoxysilane.
5. The process of claim 1 , wherein the cumulative mole ratio of alkoxysilane to olefinic halide ranges from about 1.3 to about 3.0.
6. The process of claim 1 , wherein the cumulative mole ratio of alkoxysilane to olefinic halide ranges from about 1.8 to about 2.3.
7. The process of claim 4 , wherein the cumulative mole ratio of trimethoxysilane to allyl chloride ranges from about 1.8 to about 2.3.
8. The process of claim 1 , wherein the reaction is carried out at a temperature of from about 50 to about 130° C.
9. The process of claim 1 , wherein the reaction is carried out at a temperature of from about 60 to about 80° C.
10. The method of claim 1 , wherein the ruthenium-containing catalyst is selected from the group consisting of RU 3 (CO) 12 , [Ru(CO) 3 Cl 2 ] 2 , cyclooctadiene-RuCl 2 , RuCl 3 , (Ph 3 P) 2 Ru(CO) 2 Cl 2 , (Ph 3 P) 3 Ru(CO)H 2 , Ru on Fe, Ru on Al 2 O 3 , Ru on carbon, Ru(AcAc) 3 , and RuBr 3 .
11. The process of claim 1 , wherein the amount of ruthenium present in the reaction medium is from about 5 to about 100 ppm by weight of the reactants.
12. The process of claim 1 , wherein the amount of ruthenium-containing catalyst present in the reaction medium is from about 15 to about 25 ppm by weight of the reactants.
13. The process of claim 1 , wherein the electron donating aromatic compound is selected from the group consisting of benzene, ethylbenzene, diethylbenzene, triethylbenzene, n-butylbenzene, di-t-butylbenzene, bibenzyl, toluene, t-butyltoluene, anisole, 1-phenylhexane, 1-phenyldodecane, m-xylene, mesitylene, p-cymene, diphenylmethane, triphenylmethane, phenyl ether, phenothiazine, and biphenyl.
14. The process of claim 1 wherein the electron-donating aromatic compound is present in an amount of from about 5 to about 50 mole equivalents versus the moles of ruthenium metal.
15. The process of claim 1 , wherein the electron-donating aromatic compound is present in an amount of from about 20 to about 30 mole equivalents versus the moles of ruthenium metal.
16. A process for preparing a chloroalkylmethoxysilane of the general formula:
(CH 3 ) x (CH 3 O) 3-x SiCH 2 CHR 3 CR 4 R 5 Cl
wherein R 3 is an alkyl of from 1 to 6 carbon atoms or hydrogen, R 4 is an alkyl of from 1 to 6 carbon atoms, hydrogen or chlorine, R 5 is hydrogen or an alkyl of from 1 to 6 carbon atoms and x is 0, 1 or 2, which comprises reacting an olefinic chloride of the general formula:
H 2 C═CR 3 CR 4 R 5 Cl
wherein R 3 , R 4 and R 5 have the aforestated meanings with an excess of a methoxysilane of the general formula:
(CH 3 ) x (CH 3 O) 3-x SiH
wherein x has the aforestated meaning in a cumulative mole ratio of methoxysilane to olefinic chloride of from about 1.3 to about 3.0 at a temperature of from about 60 to about 130° C. in a reaction medium into which has been added a ruthenium-containing catalyst containing from about 5 to about 100 ppm ruthenium based on the total weight of the reactants and an aromatic compound of from about 1 to about 100 mole equivalents versus the moles of ruthenium metal; wherein the yield of the chloroalkylmethoxysilane is greater than or equal to about 87 mole percent, based upon the total reaction products.
17. The process of claim 16 , wherein the olefinic chloride is allyl chloride.
18. The process of claim 16 , wherein the methoxysilane is trimethoxysilane.
19. The process of claim 18 wherein the cumulative mole ratio of methoxysilane to olefinic chloride is from about 1.3 to about 3.0.
20. The process of claim 16 wherein the reaction is carried out at a temperature of from about 60 to about 80° C.
21. The process of claim 16 wherein the ruthenium-containing catalyst is selected from the group consisting of RuCl 3 hydrate, Ru 3 (CO) 12 and [RUCl 2 (CO) 3 ] 2 .
22. The process of claim 16 wherein the reaction medium contains from about 15 to about 25 ppm ruthenium based on the total weight of the reactants.
23. The process of claim 16 wherein the olefinic chloride is allyl chloride, the methoxysilane is trimethoxysilane, the cumulative mole ratio of trimethoxysilane to allyl chloride is from about 1.4 to about 2.0, the reaction temperature is from about 60 to about 80° C., the ruthenium-containing catalyst is selected from the group consisting of RuCl 3 hydrate and the reaction medium contains from about 15 to about 25 ppm ruthenium based on the total weight of the reactants.
24. The process of claim 1 , wherein the yield of the haloorganoalkoxysilane exceeds 90 mole percent, based upon the total weight of the reaction products.
25. The process of claim 1 , wherein the yield of the haloorganoalkoxysilane exceeds 92 mole percent, based upon the total weight of the reaction products.
26. The process of claim 16 , wherein the yield of the haloorganoalkoxysilane exceeds 90 mole percent, based upon the total weight of the reaction products.
27. The process of claim 16 , wherein the yield of the haloorganoalkoxysilane exceeds 92 mole percent, based upon the total weight of the reaction products.