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US3983148A
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Process for producing cyclic siloxanes
Assignee: OSI Specialties Inc
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Filing: 1975-08-29
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Granted: 1976-09-28
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Expires: 1995-08-29
Abstract
Abstract Process for producing cyclic siloxanes by hydrolysis and condensation, the improvement comprising carrying out the process in the presence of a cationic surface active agent.
Inventors
- 👤 James Dale Reedy
- 👤 Harold D. Furbee
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-07 09:46
CPC Classifications
C; C07; C07F; C07F7/00; C07F7/02; C07F7/21
Claims Analysis
Total Claims: 14
Claim 1
Independent Claim
181 words
In a process for preparing cyclic siloxane compounds, said process consisting essentially of the hydrolysis and condensation of a hydrolyzable organosilicon compound, the improvement comprising increasing the yield of said cyclic siloxane compounds by hydrolyzing and condensing said organosilicon compound in the presence of a cationic surface active agent, said agent being essentially soluble only in the aqueous phase of said process, wherein the concentration of the cationic surface active agent in said aqueous phase is from about 0.01 to about 10 weight percent, wherein said cationic surface active agent is selected from the class consisting of a salt of a protonated amine, a quaternary ammonium salt, a salt of a protonated carboxylic acid, a salt of a protonated alcohol, a salt of a protonated nitrile, a salt of a protonated sulfoxide, a salt of a protonated mercaptan, a quaternary phosphonium salt, and a salt of a protonated phosphine, wherein the cation of each salt contains from 5 to 30 carbon atoms, and wherein the anion of each salt is selected from the group consisting of halide, sulfate, and phosphate anions.
Claim 2
Dependent Claim
181 words
In a process for preparing cyclic siloxane compounds, said process consisting essentially of the hydrolysis and condensation of a hydrolyzable organosilicon compound, the improvement comprising increasing the yield of said cyclic siloxane compounds by hydrolyzing and condensing said organosilicon compound in the presence of a cationic surface active agent, said agent being essentially soluble only in the aqueous phase of said process, wherein the concentration of the cationic surface active agent in said aqueous phase is from about 0.01 to about 10 weight percent, wherein said cationic surface active agent is selected from the class consisting of a salt of a protonated amine, a quaternary ammonium salt, a salt of a protonated carboxylic acid, a salt of a protonated alcohol, a salt of a protonated nitrile, a salt of a protonated sulfoxide, a salt of a protonated mercaptan, a quaternary phosphonium salt, and a salt of a protonated phosphine, wherein the cation of each salt contains from 5 to 30 carbon atoms, and wherein the anion of each salt is selected from the group consisting of halide, sulfate, and phosphate anions.
Claim 3
Dependent Claim
44 words
A process as defined in claim 1 wherein said process is carried out in the absence of a solvent and wherein the cationic surface active agent is a salt of a protonated amine and wherein the anion of said salt is a chloride anion.
Claim 4
Dependent Claim
29 words
A process as defined in claim 2 wherein the concentration of the cationic surface active agent in said aqueous phase is from about 0.5 to about 2 weight percent.
Claim 5
Dependent Claim
130 words
A process as defined in claim 2 wherein the cationic surface active agent is formed in situ by employing an aqueous phase that contains hydrochloric acid and a precursor amine selected from the class consisting of primary amines of the formula RNH 2 wherein R is a monovalent hydrocarbon radical having 6 to 10 carbon atoms, secondary amines of the formula R 2 NH wherein R is a monovalent hydrocarbon radical wherein the sum number of the carbon atoms of both R radicals of the secondary amine ranges from 6 to 14; and tertiary amines of the formula R 3 N wherein R is a monovalent hydrocarbon radical wherein the sum number of the carbon atoms of all three R radicals of the tertiary amine ranges from 9 to 18.
Claim 6
Dependent Claim
13 words
A process as defined in claim 4 wherein R is an n-alkyl radical.
Claim 7
Dependent Claim
17 words
A process as defined in claim 5 wherein the cationic surface active agent is a primary amine.
Claim 8
Dependent Claim
13 words
A process as defined in claim 6 wherein the primary amine is n-octylamine.
Claim 9
Dependent Claim
15 words
A process as defined in claim 4 that is carried out in a continuous manner.
Claim 10
Dependent Claim
100 words
A process as defined in claim 2 wherein the hydrolyzable organosilicon compound is selected from the class consisting of silanes of the formula R.sub.n Si-X.sub.4-n wherein R represents a radical selected from the class consisting of hydrogen and a monovalent hydrocarbon radical n has a value of 0 to 3 and X is a hydrolyzable group; siloxanes of the formula (X)R.sub.2 SiO(R.sub.2 SiO).sub.x SiR.sub.2 (X) wherein R and X are the same as defined above and x has a value of 0 to 3; and silylamines of the formula ##STR2##wherein R, X and x are the same as defined above.
Claim 11
Dependent Claim
51 words
A process as defined in claim 4 wherein the hydrolyzable organosilicon compound is a silane of the formula R.sub.n -Si-X.sub.4-n wherein R represents a radical selected from the class consisting of hydrogen and a monovalent hydrocarbon radical, n has a value of 0 to 3 and X is a hydrolyzable group.
Claim 12
Dependent Claim
20 words
A process as defined in claim 10, wherein R is methyl, n is 2 and X is a chlorine radical.
Claim 13
Dependent Claim
34 words
A process as defined in claim 5, wherein the hydrolyzable organosilicon compound is selected from the class consisting of dichlorodimethylsilane, a mixture of dichlorodimethylsilane and dichloromethylsilane, and a mixture of dichlorodimethylsilane, dichloromethylsilane and chlorotrimethylsilane.
Claim 14
Dependent Claim
14 words
A process as defined in claim 7 wherein the hydrolyzable organosilicon compound is dichlorodimethylsilane.
References Cited (Backward Citations)
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-09-28 | 1980-03-29 | 1980-09-28 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-09-28 | 1984-03-29 | 1984-09-28 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-09-28 | 1988-03-29 | 1988-09-28 | $7700.00 | Window Closed / Lapsed |