US4975510A
Expired / Lapsed
US
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Process for preparing diorganopolysiloxanes having terminal triorganosiloxy units
Assignee: Wacker Chemie AG
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Filing: 1988-11-14
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Granted: 1990-12-04
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Expires: 2008-11-14
Abstract
Abstract A process for preparing diorganopolysiloxanes containing terminal triorganosiloxy groups which comprises reacting in a 1st step, a cyclic diorganopolysiloxane and/or diorganodichlorosilane hydrolyzate with from 0.05 to 3 percent by weight of triorganochlorosilane, based on the weight of the cyclic diorganopolysiloxane and/or diorganodichlorosilane hydrolyzate employed in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the total weight of the organosilicon compounds employed, to form a reaction mixture containing α-triorganosiloxy-ω-chlorodiorganopolysiloxane, and in a 2nd step, adding to the reaction mixture obtained in the 1st step and containing the α-triorganosiloxy-ω-chlorodiorganopolysiloxane, a diorganopolysiloxane having one Si-bonded hydroxyl group in each of the terminal units in an amount of from 1 to 1.2 gram-moles of Si-bonded hydroxyl group in this diorganopolysiloxane per gram-atom of Si-bonded chlorine in the triorganochlorosilane, and in a 3rd step, adding hexaorganodisilazane to the reaction mixture of the 2nd step in order to deactivate the phosphonitrile chloride and remove hydrogen chloride from the diorganopolysiloxanes containing terminal triorganosiloxy groups and thereafter removing the low-boiling components by distillation.
Inventors
- 👤 Karl-Heinrich Wegehaupt
- 👤 Karl Braunsperger
- 👤 Jorg Patzke
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 14:57
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/32; C08G77/06; C08G77/20
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
192 words
A process for preparing diorganopolysiloxanes containing terminal vinyldiorganosiloxy groups which comprises in a 1st step, reacting an organosilicon compound selected from the group consisting of a cyclic diorganopolysiloxane, a diorganodichlorosilane hydrolyzate and mixtures thereof with from 0.05 to 3 percent by weight of vinyldiorganochlorosilane, based on the weight of the organosilicon compound, in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the weight of the organosilicon compound and the vinyldiorganochlorosilane employed to form a reaction mixture containing α-vinyldiorganosiloxy-ω-chlorodiorganopolysiloxane and in a 2nd step, adding to the reaction mixture obtained in the 1st step and containing the α-vinyldiorganosiloxy-ω-chlorodiorganopolysiloxane, a diorganopoly siloxane having one Si-bonded hydroxyl group in each of the terminal units in an amount of from 1 to 1.2 gram-moles of Si-bonded hydroxyl group in the diorganopolysiloxane per gram-atom of Si-bonded chlorine in the, vinyldiorganochlorosilane and in a 3rd step, adding hexaorganodisilazane to the reaction mixture of the 2nd step in order to deactivate the phosphonitrile chloride and remove hydrogen chloride from the diorganopolysiloxane containing terminal vinyldiorganosiloxy groups and removing low-boiling components which boil at 140° to 150° at 0.5 to 8 hPa by distillation.
Claim 2
Dependent Claim
192 words
A process for preparing diorganopolysiloxanes containing terminal vinyldiorganosiloxy groups which comprises in a 1st step, reacting an organosilicon compound selected from the group consisting of a cyclic diorganopolysiloxane, a diorganodichlorosilane hydrolyzate and mixtures thereof with from 0.05 to 3 percent by weight of vinyldiorganochlorosilane, based on the weight of the organosilicon compound, in the presence of from 1 to 50 ppm by weight of phosphonitrile chloride, based on the weight of the organosilicon compound and the vinyldiorganochlorosilane employed to form a reaction mixture containing α-vinyldiorganosiloxy-ω-chlorodiorganopolysiloxane and in a 2nd step, adding to the reaction mixture obtained in the 1st step and containing the α-vinyldiorganosiloxy-ω-chlorodiorganopolysiloxane, a diorganopoly siloxane having one Si-bonded hydroxyl group in each of the terminal units in an amount of from 1 to 1.2 gram-moles of Si-bonded hydroxyl group in the diorganopolysiloxane per gram-atom of Si-bonded chlorine in the, vinyldiorganochlorosilane and in a 3rd step, adding hexaorganodisilazane to the reaction mixture of the 2nd step in order to deactivate the phosphonitrile chloride and remove hydrogen chloride from the diorganopolysiloxane containing terminal vinyldiorganosiloxy groups and removing low-boiling components which boil at 140° to 150° at 0.5 to 8 hPa by distillation.
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
115 words
The process of claim 1, wherein the diorganodichlorosilane hydrolyzate employed is one which comprises from 20 to 30 percent by weight of a cyclic diorganopolysiloxane of the formula (R.sub.2 SiO).sub.n and 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 hydrolyzate employed, in which 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, n is an integer having a value of from 3 to 11 and m is an integer having a value of from 20 to 50.
Claim 5
Dependent Claim
10 words
The process of claim 1, wherein the vinyldiorganochlorosilane is vinyldimethylchorosilane.
Claim 6
Dependent Claim
72 words
The process of claim 1, wherein the diorganopolysiloxane containing one Si-bonded hydroxyl group in each of the terminal units has the formula HO(R.sub.2 SiO).sub.p SiR.sub.2 OH 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 p is an integer having a value of from 8 to 13.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1993-12-03 | 1994-06-04 | 1994-12-04 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1997-12-03 | 1998-06-04 | 1998-12-04 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2001-12-03 | 2002-06-04 | 2002-12-04 | $7700.00 | Window Closed / Lapsed |