Linear and cyclic siloxanes and cosmetic compositions made thereof
US-9221952-B2 · Dec 29, 2015 · US
US10017526B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10017526-B2 |
| Application number | US-201515322775-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 29, 2015 |
| Priority date | Jul 1, 2014 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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Cyclic siloxanes are prepared economically by reaction of an alkali metal siliconate having a mol ratio of alkali metal cation to silicon of less than one or their hydrolysis/condensation products or mixture thereof, with a halosilane.
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The invention claimed is: 1. A process for preparing cyclic siloxanes of the formula (1) [RSi(OSiR 1 R 2 R 3 )O] n (1), comprising: reacting alkali metal salts of silanols of the formula (2), R—Si(OH) 3-m (OM) m (2), wherein m is 0, 1, 2, or 3, and over all species of the alkali metal salts of silanols of the formula (2), m is on average 0.1 to <1, their hydrolysis/condensation products, or alkali metal salts of silanols of the formula (2) together with their hydrolysis/condensation products, wherein the molar ratio of cation M to silicon is <1, with halosilanes of the formula (3) R 1 R 2 R 3 Si-Hal (3) where n is 3, 4, 5, 6, 7 or 8, R is an organic radical bonded via carbon to silicon, M is an alkali metal cation, Hal is a halogen radical, and R 1 , R 2 , and R 3 are hydrogen, C 1-10 alkoxy radicals, C 1-20 aryloxy radicals or monovalent hydrocarbon radicals having 1 to 18 carbon atoms which are unsubstituted or substituted by halogen atoms or alkoxy groups, and thereby producing cyclic siloxanes of the formula (1). 2. The process of claim 1 , wherein R is a monovalent, Si—C-bonded hydrocarbon radical having 1 to 30 carbon atoms, which is unsubstituted or substituted by halogen atoms, C 1-6 alkyl or C 1-6 alkoxy groups or silyl groups, and in which one or more mutually nonadjacent —CH 2 — units are optionally replaced by —O— or —S—. 3. The process of claim 1 , wherein M comprises sodium, potassium, or a mixture thereof. 4. The process of claim 2 , wherein M comprises sodium, potassium, or a mixture thereof. 5. The process of claim 1 , wherein the molar ratio M:Si in formula (2) is from 0.4 to 0.85. 6. The process of claim 2 , wherein the molar ratio M:Si in formula (2) is from 0.4 to 0.85. 7. The process of claim 3 , wherein the molar ratio M:Si in formula (2) is from 0.4 to 0.85. 8. The process of claim 1 , wherein the halosilanes of formula (3) are chlorosilanes. 9. The process of claim 2 , wherein the halosilanes of formula (3) are chlorosilanes. 10. The process of claim 3 , wherein the halosilanes of formula (3) are chlorosilanes. 11. The process of claim 5 , wherein the halosilanes of formula (3) are chlorosilanes. 12. The process of claim 1 , wherein reacting is carried out at 0° C. to 120° C. 13. The process of claim 2 , wherein reacting is carried out at 0° C. to 120° C. 14. The process of claim 3 , wherein reacting is carried out at 0° C. to 120° C. 15. The process of claim 5 , wherein reacting is carried out at 0° C. to 120° C. 16. The process of claim 8 , wherein reacting is carried out at 0° C. to 120° C. 17. The process of claim 1 , wherein reacting is carried out without auxiliary base. 18. The process of claim 2 , wherein reacting is carried out without auxiliary base. 19. The process of claim 3 , wherein reacting is carried out without auxiliary base. 20. The process of claim 5 , wherein reacting is carried out without auxiliary base. 21. The process of claim 1 , wherein n is 4.
Cyclic compounds having at least one ring containing silicon, but no carbon in the ring · CPC title
Preparation and treatment thereof · CPC title
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