GB1080397A - Distillable siloxymethylsiloxyl compound,and process for its production - Google Patents
Distillable siloxymethylsiloxyl compound,and process for its productionInfo
- Publication number
- GB1080397A GB1080397A GB31283/66A GB3128366A GB1080397A GB 1080397 A GB1080397 A GB 1080397A GB 31283/66 A GB31283/66 A GB 31283/66A GB 3128366 A GB3128366 A GB 3128366A GB 1080397 A GB1080397 A GB 1080397A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- gives
- product
- hydroxymethyl
- recovering
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000034 method Methods 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 abstract 1
- PGBKOXQSNCIJSE-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3,2,4-dioxadisilolane Chemical compound C[Si]1(C)CO[Si](C)(C)O1 PGBKOXQSNCIJSE-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- JOVDRTJIBGMLLC-UHFFFAOYSA-N [[[[hydroxymethyl(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]oxy-dimethylsilyl]methanol Chemical compound OC[Si](O[Si](O[Si](O[Si](CO)(C)C)(C)C)(C)C)(C)C JOVDRTJIBGMLLC-UHFFFAOYSA-N 0.000 abstract 1
- SVZSOVXXWFZQHH-UHFFFAOYSA-N [[hydroxymethyl(dimethyl)silyl]oxy-dimethylsilyl]methanol Chemical compound OC[Si](C)(C)O[Si](C)(C)CO SVZSOVXXWFZQHH-UHFFFAOYSA-N 0.000 abstract 1
- ZBVZYBWFESOWPG-UHFFFAOYSA-N [acetyloxy(dimethyl)silyl]methyl acetate Chemical compound CC(=O)OC[Si](C)(C)OC(C)=O ZBVZYBWFESOWPG-UHFFFAOYSA-N 0.000 abstract 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 abstract 1
- UPKHMNVQWIFQBW-UHFFFAOYSA-N bromomethyl-[bromomethyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound BrC[Si](C)(C)O[Si](C)(C)CBr UPKHMNVQWIFQBW-UHFFFAOYSA-N 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- YYLGKUPAFFKGRQ-UHFFFAOYSA-N dimethyldiethoxysilane Chemical compound CCO[Si](C)(C)OCC YYLGKUPAFFKGRQ-UHFFFAOYSA-N 0.000 abstract 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 229910017464 nitrogen compound Inorganic materials 0.000 abstract 1
- 150000002830 nitrogen compounds Chemical class 0.000 abstract 1
- 229920006324 polyoxymethylene Polymers 0.000 abstract 1
- -1 polyoxymethylenes Polymers 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0838—Compounds with one or more Si-O-Si sequences
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0046845 | 1965-08-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1080397A true GB1080397A (en) | 1967-08-23 |
Family
ID=7101277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31283/66A Expired GB1080397A (en) | 1965-08-07 | 1966-07-12 | Distillable siloxymethylsiloxyl compound,and process for its production |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3444228A (enExample) |
| BE (1) | BE685083A (enExample) |
| DE (1) | DE1493733A1 (enExample) |
| GB (1) | GB1080397A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009046254A1 (de) * | 2009-10-30 | 2011-05-19 | Wacker Chemie Ag | Verfahren zur Herstellung von (Hydroxymethyl)polysiloxanen |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2983744A (en) * | 1955-11-17 | 1961-05-09 | Du Pont | Heterocycles |
| US3256308A (en) * | 1962-03-05 | 1966-06-14 | Dow Chemical Co | 2-methyl-1, 3-dioxa-2-sila-cyclohept-5-ene |
| US3328340A (en) * | 1963-09-09 | 1967-06-27 | Gen Electric | Organopolysiloxane composition of reduced structure |
-
1965
- 1965-08-07 DE DE19651493733 patent/DE1493733A1/de active Pending
-
1966
- 1966-07-06 US US563065A patent/US3444228A/en not_active Expired - Lifetime
- 1966-07-12 GB GB31283/66A patent/GB1080397A/en not_active Expired
- 1966-08-04 BE BE685083D patent/BE685083A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1493733A1 (de) | 1969-11-20 |
| BE685083A (enExample) | 1967-01-16 |
| US3444228A (en) | 1969-05-13 |
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