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US4658006A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for the preparation of alkoxy-containing organopolysiloxane

Assignee: Shin-Etsu Chemical Co Ltd
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Filing: 1986-03-31
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Granted: 1987-04-14
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Expires: 2006-03-31
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Abstract

Abstract A diorganopolysiloxane terminated at both molecular chain ends each with a monohydrocarbyl dialkoxy silyl group, which is useful as a base ingredient in room temperature-curable silicone rubber compositions, is prepared by first reacting a silanol-terminated diorganopolysiloxane with a monohydrocarbyl tri(ketoxime) silane to replace the silanolic hydroxy group with a monohydrocarbyl di(ketoxime) siloxy group and then reacting the oxime-terminated diorganopolysiloxane with a monohydric alcohol, e.g. methyl alcohol, to replace the ketoxime groups with alkoxy groups. The reactions can proceed under very mild conditions without any catalyst so that the desired alkoxy-terminated diorganopolysiloxane is obtained in a high purity.

Inventors

  • 👤 Yoshio Inoue

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 06:45
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/14; C08G77/18; C08G77/22; C08G77/26; C08G77/38

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 278 words
A method for the preparation of an alkoxy-terminated organopolysiloxane which comprises the successive steps of: (a) reacting a silanol-terminated diorganopolysiloxane represented by the general formula HO--SiR.sup.1.sub.2 --O.sub.n H, in which each R 1 is a monovalent group selected from the class consisting of methyl, vinyl, phenyl and 3,3,3-trifluoropropyl groups and the subscript n is a positive integer, with an organosilane compound represented by the general formula R.sup.3 Si(O--N═X).sub.3, in which R 3 is a monovalent group selected from the class consisting of methyl, ethyl, propyl, vinyl, phenyl and 3,3,3-trifluoropropyl groups and X is a divalent group represented by the general formula ═CR 4 2 , R 4 being a halogen-substituted or unsubstituted monovalent hydrocarbon group, or ##STR5## R 5 being a halogen-substituted or unsubstituted divalent hydrocarbon group, in a molar ratio of the silane compound to the silanol groups in the diorganopolysiloxane of at least 1 under a substantially anhydrous condition to form an intermediate oxime-terminated diorganopolysiloxane represented by the general formula (X═N--O).sub.2 (R.sup.3)Si--O--SiR.sup.1.sub.2 --O.sub.n Si(R.sup.3)(O--N═X).sub.2, in which R 1 , R 3 , X and n each have the same meaning as defined above; and (b) reacting the intermediate oxime-terminated diorganopolysiloxane with a monohydric alcohol represented by the general formula R.sup.6 OH, in which R 6 is a monovalent hydrocarbon group having 1 to 8 carbon atoms, in a molar ratio of the monohydric alcohol to the oxime groups of the formula --O--N═X in the intermediate oxime-terminated diorganopolysiloxane of at least 1 to form an alkoxy-terminated diorganopolysiloxane represented by the general formula (R.sup.6 O).sub.2 (R.sup.3)Si--O--SiR.sup.1.sub.2 --O.sub.n Si(R.sup.3)(OR.sup.6).sub.2, in which R 1 , R 3 , R 6 and n each have the same meaning as defined above.
Claim 2
Independent Claim 278 words
A method for the preparation of an alkoxy-terminated organopolysiloxane which comprises the successive steps of: (a) reacting a silanol-terminated diorganopolysiloxane represented by the general formula HO--SiR.sup.1.sub.2 --O.sub.n H, in which each R 1 is a monovalent group selected from the class consisting of methyl, vinyl, phenyl and 3,3,3-trifluoropropyl groups and the subscript n is a positive integer, with an organosilane compound represented by the general formula R.sup.3 Si(O--N═X).sub.3, in which R 3 is a monovalent group selected from the class consisting of methyl, ethyl, propyl, vinyl, phenyl and 3,3,3-trifluoropropyl groups and X is a divalent group represented by the general formula ═CR 4 2 , R 4 being a halogen-substituted or unsubstituted monovalent hydrocarbon group, or ##STR5## R 5 being a halogen-substituted or unsubstituted divalent hydrocarbon group, in a molar ratio of the silane compound to the silanol groups in the diorganopolysiloxane of at least 1 under a substantially anhydrous condition to form an intermediate oxime-terminated diorganopolysiloxane represented by the general formula (X═N--O).sub.2 (R.sup.3)Si--O--SiR.sup.1.sub.2 --O.sub.n Si(R.sup.3)(O--N═X).sub.2, in which R 1 , R 3 , X and n each have the same meaning as defined above; and (b) reacting the intermediate oxime-terminated diorganopolysiloxane with a monohydric alcohol represented by the general formula R.sup.6 OH, in which R 6 is a monovalent hydrocarbon group having 1 to 8 carbon atoms, in a molar ratio of the monohydric alcohol to the oxime groups of the formula --O--N═X in the intermediate oxime-terminated diorganopolysiloxane of at least 1 to form an alkoxy-terminated diorganopolysiloxane represented by the general formula (R.sup.6 O).sub.2 (R.sup.3)Si--O--SiR.sup.1.sub.2 --O.sub.n Si(R.sup.3)(OR.sup.6).sub.2, in which R 1 , R 3 , R 6 and n each have the same meaning as defined above.
Claim 3
Dependent Claim 29 words
The method for the preparation of an alkoxy-terminated organopolysiloxane as claimed in claim 1 wherein the subscript n is a positive integer in the range from 20 to 1000.
Claim 4
Dependent Claim 24 words
The method for the preparation of an alkoxy-terminated organopolysiloxane as claimed in claim 1 wherein R 4 is a methyl or an ethyl group.
Claim 5
Dependent Claim 33 words
The method for the preparation of an alkoxy-terminated organopolysiloxane as claimed in claim 1 wherein R 5 is a butylene group of the formula --CH 2 CH 2 CH 2 CH 2 --.
Claim 6
Dependent Claim 21 words
The method for the preparation of an alkoxy-terminated organopolysiloxane as claimed in claim 1 wherein the monohydric alcohol is methyl alcohol.
Claim 7
Dependent Claim 35 words
The method for the preparation of an alkoxy-terminated organopolysiloxane as claimed in claim 1 wherein the reaction of the step (b) is performed at a temperature in the range from 50° to 100 ° C.

References Cited (Backward Citations)

US3344160A Cited
US4426480A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-04-13 1990-10-13 1991-04-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-04-13 1994-10-13 1995-04-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-04-13 1998-10-13 1999-04-14 $7700.00 Window Closed / Lapsed

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