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US4228092A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of organoalkoxysilanes

Assignee: Dynamit Nobel AG
•
Filing: 1979-01-02
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Granted: 1980-10-14
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Expires: 1999-01-02
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Abstract

Abstract An improvement in a process for the esterification of a organochlorosilane by feeding alcohol into a chlorosilane maintained within a reaction zone without said alcohol contacting said chlorosilane in the gas phase wherein the esterification is performed stepwise with extraction of hydrogen chloride which has developed, the improvement which comprises employing in at least a final esterification step an organochlorosilane of the formula H.sub.a R.sub.b SiCl.sub.4-a-b wherein R represents an optionally halogen-substituted alkyl radical which can also contain an oxygen or sulfur atom in the chain, or a halogen or a NO 2 group or a protected phenolic group containing aryl radical, a equals 0, 1, or 2, b equals 1 or 2, and a+b amounts to a maximum of 3, said final esterification step being performed with the addition of heat.

Inventors

  • 👤 Hans-Joachim Kotzsch
  • 👤 Claus-Dietrich Seiler
  • 👤 Hans-Joachim Vahlensieck

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 19:58
CPC Classifications
C; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/18; C07F7/1804; C07F7/1872; C07F7/188; C07F7/025

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 148 words
An improvement in a process for the esterification of an organochlorosilane by feeding alcohol into a chlorosilane maintained within a reaction zone without said alcohol contacting said chlorosilane in the gas phase wherein the esterification is performed stepwise with extraction of hydrogen chloride which has developed, the improvement which comprises employing in at least a final esterification step an organochlorosilane of the formula H.sub.a R.sub.b Si Cl.sub.4-a-b wherein R represents an optionally halogen-substituted alkyl radical which can also contain an oxygen or sulfur atom in the chain or a halogen or a NO 2 group or a protected phenolic group containing aryl radical a equals 0, 1, or 2, b equals 1 or 2, and a+b amounts to a maximum of 3, said final esterification step being performed with the addition of heat, said final esterification step being carried out at the boiling temperature of the reaction mixture.
Claim 2
Dependent Claim 148 words
An improvement in a process for the esterification of an organochlorosilane by feeding alcohol into a chlorosilane maintained within a reaction zone without said alcohol contacting said chlorosilane in the gas phase wherein the esterification is performed stepwise with extraction of hydrogen chloride which has developed, the improvement which comprises employing in at least a final esterification step an organochlorosilane of the formula H.sub.a R.sub.b Si Cl.sub.4-a-b wherein R represents an optionally halogen-substituted alkyl radical which can also contain an oxygen or sulfur atom in the chain or a halogen or a NO 2 group or a protected phenolic group containing aryl radical a equals 0, 1, or 2, b equals 1 or 2, and a+b amounts to a maximum of 3, said final esterification step being performed with the addition of heat, said final esterification step being carried out at the boiling temperature of the reaction mixture.
Claim 3
Dependent Claim 28 words
A process according to claim 1 wherein the reaction mixture is maintained at a boiling temperature after sufficient alcohol has been added to esterify the last chlorine atom.
Claim 4
Dependent Claim 20 words
A process according to claim 1 wherein the esterification is carried out in the absence of an acid binding agent.
Claim 5
Dependent Claim 33 words
A process according to claim 1 wherein R is an alkyl radical of 1 to 8 carbon atoms which can be halogen-substituted or can contain an oxygen or sulfur atoms in the chain.
Claim 6
Dependent Claim 22 words
A process according to claim 1 wherein R is an aryl radical containing a halogen or a phenolic or a nitro group.
Claim 7
Dependent Claim 68 words
A process according to claim 1 wherein said organochlorosilane is selected from the group consisting of methyltrichlorosilane, hydrogenmethyldichlorosilane, hydrogendimethylchlorosilane, dimethyldichlorosilane, trimethylchlorosilane, ethyltrichlorosilane, hydrogenethyldichlorosilane, propyltrichlorosilane, n- and isobutyltrichlorosilane, amyltrichlorosilane, n-octyltrichlorosilane, 2-ethylhexyltrichlorosilane, n-dodecyltrichlorosilane, n-octadecyltrichlorosilane, vinyltrichlorosilane, vinylmethyldichlorosilane, vinyldimethylchlorosilane, allyltrichlorosilane, 2-cyclohexenylethyltrichlorosilane, butenyltrichlorosilane, 3-allyloxypropyltrichlorosilane, benzyltrichlorosilane, benzylmethyldichlorosilane, 2-phenylethyltrichlorosilane, 3-phenoxypropyltrichlorosilane, 3-4'-isopropylphenoxypropyltrichlorosilane, phenyltrichlorosilane, phenylmethyldichlorosilane, diphenyldichlorosilane, chlormethyldimethylchlorosilane, chlormethylmethyldichlorosilane, chlormethyltrichlorosilane, brommethyltrichlorosilane, 2-chlorethyltrichlorosilane, 2-chlorethylmethyldichlorosilane, 3-chlorpropyltrichlorosilane, 3-chlorpropylmethyldichlorosilane, 3-brompropyltrichlorosilane, 3-iodinepropyltrichlorosilane, 3-fluorpropyltrichlorosilane, 3,3,3-trichloropropyltrichlorosilane, 3,3,3-trichloropropylmethyldichlorosilane, 3,3,3-trifluorpropyltrichlorosilane, 4'-isopropylphenoxymethylmethyldichlorosilane, pentabrombenzyltrichlorosilane, 3-pentachlorophenoxypropyltrichlorosilane, 3-2'4'-dichlorophenoxypropyltrichlorosilane, 3-p-nitrophenoxypropyltrichlorosilane and 3-o-methoxyphenoxypropyltrichlorosilane.
Claim 8
Dependent Claim 19 words
A process according to claim 1 wherein said alcohol is an aliphatic alcohol having 1 to 20 carbon atoms.
Claim 9
Dependent Claim 44 words
A process according to claim 7 wherein said alcohol is selected from the group consisting of methanol, n-propanol, a butanol, a pentanol, a hexanol, a heptanol, an octanol, a nonanol, a decanol, an undecanol, 2-methoxyethanol, 2-ethoxyethanol, 2-butoxyethanol, diethylglycolmonomethyl ether, diethyleneglycolmonobutyl ether and tetraethyleneglycolmonomethyl ether.

References Cited (Backward Citations)

US3651117A Cited
US3792071A Cited
US3985781A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-10-14 1984-04-14 1984-10-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-10-14 1988-04-14 1988-10-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-10-14 1992-04-14 1992-10-14 $7700.00 Window Closed / Lapsed

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