US4902813A
Expired / Lapsed
US
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Process for preparing diorganopolysiloxanes having terminal Si-bonded hydroxyl groups
Assignee: Wacker Chemie AG
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Filing: 1988-12-07
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Granted: 1990-02-20
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Expires: 2008-12-07
Abstract
Abstract A process for preparing diorganopolysiloxanes having terminal Si-bonded hydroxyl groups which comprises reacting an organosilicon compound selected from a cyclic diorganopolysiloxane, a diorganodichlorosilane hydrolysis product and mixtures thereof with from 0.1 to 3 percent by weight of a diorganodichlorosilane, based on the weight of the organosilicon compound, i.e., the cyclic diorganopolysiloxane and/or diorganodichlorosilane hydrolysis product employed, in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the total weight of the organosilicon compound and diorganodichlorosilane employed, to form diorganopolysiloxanes containing an Si-bonded chlorine atom in each of the terminal units, then treating the reaction mixture with water or an aqueous solution, separating off the aqueous phase from the diorganopolysiloxanes containing an Si-bonded hydroxyl group in each of the terminal units and thereafter removing the low boiling constituents by distillation.
Inventors
- 👤 Karl-Heinrich Wegehaupt
- 👤 Karl Braunsperger
- 👤 Gunter von Au
- 👤 Fridolin Stary
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 21:13
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/14; C08G77/16; C08G77/32; C08G77/34
Claims Analysis
Total Claims: 8
Claim 1
Independent Claim
120 words
A process for preparing diorganopolysiloxaneshaving terminal Si-bonded hydroxyl groups which comprises reacting an organosilicon compound selected from the group consisting of a cyclic diorganopolysiloxane, a diorganodichlorosilane hydrolysis product and mixtures thereof with from 0.1 to 3 percent by weight of diorganodichlorosilane, based on the weight of the organosilicon compound employed, in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the total weight of the organosilicon compound and diorganodichlorosilane employed, to form diorganopolysiloxanes containing an Si-bonded chlorine atom in each of the terminal units, treating the reaction mixture with water or an aqueous solution, removing the aqueous phase and thereafter distilling off the low boiling constituents from the diorganopolysiloxanes containing terminal Si-bonded hydroxyl groups.
Claim 2
Dependent Claim
120 words
A process for preparing diorganopolysiloxaneshaving terminal Si-bonded hydroxyl groups which comprises reacting an organosilicon compound selected from the group consisting of a cyclic diorganopolysiloxane, a diorganodichlorosilane hydrolysis product and mixtures thereof with from 0.1 to 3 percent by weight of diorganodichlorosilane, based on the weight of the organosilicon compound employed, in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the total weight of the organosilicon compound and diorganodichlorosilane employed, to form diorganopolysiloxanes containing an Si-bonded chlorine atom in each of the terminal units, treating the reaction mixture with water or an aqueous solution, removing the aqueous phase and thereafter distilling off the low boiling constituents from the diorganopolysiloxanes containing terminal Si-bonded hydroxyl groups.
Claim 3
Dependent Claim
60 words
The process of claim 1, wherein the cyclic diorganopolysiloxane has the formula (R.sub.2 SiO).sub.n where R is selected from the group consisting of hydrocarbon radicals having from 1 to 18 carbon atoms per radical and halogenated hydrocarbon radicals having from 1 to 18 carbon atoms per radical and n is an integer having a value of from 3 to 11.
Claim 4
Dependent Claim
112 words
The process of claim 1, wherein the diorganodichlorosilane hydrolysis product consists of 20 to 30 percent by weight of a cyclic diorganopolysiloxane of the formula (R.sub.2 SiO).sub.n and from 70 to 80 percent by weight of a diorganopolysiloxane of the formula HO(R.sub.2 SiO).sub.m SiR.sub.2 OH based on the weight of the diorganodichlorosilane hydrolysis product employed, R is selected from the group consisting of hydrocarbon radicals having from 1 to 18 carbon atoms per radical and halogenated hydrocarbon radicals having from 1 to 18 carbon atoms per radical, m is an integer having a value of from 20 to 50 and n is an integer having a value of from 3 to 11.
Claim 5
Dependent Claim
46 words
The process of claim 1, wherein the diorganodichlorosilane has the formula R.sub.2 SiCl.sub.2 wherein R is selected from the group consisting of hydrocarbon radicals having from 1 to 18 carbon atoms per radical and halogenated hydrocarbon radicals having from 1 to 18 carbon atoms per radical.
Claim 6
Dependent Claim
36 words
The process of claim 1, wherein the diorganopolysiloxanes containing an Si-bonded hydroxyl group in each of the terminal units are separated from constituents which boil at 140° to 150° C. under 0.5 to 8 hPa (absolute).
Claim 7
Dependent Claim
35 words
The process of claim 2, wherein the diorganopolysiloxanes containing an Si-bonded hydroxyl group in each of the terminal units are separated from constituents which boil at 140° to 150° C. under 0.5 to hPa (absolute).
Claim 8
Dependent Claim
36 words
The process of claim 3, wherein the diorganopolysiloxanes containing an Si-bonded hydroxyl group in each of the terminal units are separated from constituents which boil at 140° to 150° C. under 0.5 to 8 hPa (absolute).
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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) | 1993-02-19 | 1993-08-21 | 1994-02-20 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1997-02-19 | 1997-08-21 | 1998-02-20 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2001-02-19 | 2001-08-21 | 2002-02-20 | $7700.00 | Window Closed / Lapsed |