GB971569A - Improvements in or relating to organosilanes and their preparation - Google Patents
Improvements in or relating to organosilanes and their preparationInfo
- Publication number
- GB971569A GB971569A GB2832262A GB2832262A GB971569A GB 971569 A GB971569 A GB 971569A GB 2832262 A GB2832262 A GB 2832262A GB 2832262 A GB2832262 A GB 2832262A GB 971569 A GB971569 A GB 971569A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- ethoxymethyl
- produce
- reaction
- chloride
- 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
- 150000001282 organosilanes Chemical class 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 abstract 6
- FCYRSDMGOLYDHL-UHFFFAOYSA-N chloromethoxyethane Chemical compound CCOCCl FCYRSDMGOLYDHL-UHFFFAOYSA-N 0.000 abstract 6
- -1 Organosilane ethers Chemical class 0.000 abstract 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 4
- 239000011777 magnesium Substances 0.000 abstract 4
- 229910052749 magnesium Inorganic materials 0.000 abstract 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 abstract 2
- 239000012346 acetyl chloride Substances 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 abstract 2
- 229960002523 mercuric chloride Drugs 0.000 abstract 2
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 abstract 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- 239000011592 zinc chloride Substances 0.000 abstract 2
- 235000005074 zinc chloride Nutrition 0.000 abstract 2
- CRTUFWNZYJUOTB-UHFFFAOYSA-N (hydroxymethyl-methyl-propylsilyl)methanol Chemical compound CCC[Si](C)(CO)CO CRTUFWNZYJUOTB-UHFFFAOYSA-N 0.000 abstract 1
- GTXRCVNPJGWSST-UHFFFAOYSA-N C(C)OC[Si](C)(COCC)COCC Chemical compound C(C)OC[Si](C)(COCC)COCC GTXRCVNPJGWSST-UHFFFAOYSA-N 0.000 abstract 1
- VYPKAPJPWDDWIS-UHFFFAOYSA-N C(C)OC[Si](C1=CC=CC=C1)(C1=CC=CC=C1)COCC Chemical compound C(C)OC[Si](C1=CC=CC=C1)(C1=CC=CC=C1)COCC VYPKAPJPWDDWIS-UHFFFAOYSA-N 0.000 abstract 1
- PGGGFWRVCZEIFS-UHFFFAOYSA-N C(C)OC[Si](C1CCCCC1)(COCC)COCC Chemical compound C(C)OC[Si](C1CCCCC1)(COCC)COCC PGGGFWRVCZEIFS-UHFFFAOYSA-N 0.000 abstract 1
- XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 abstract 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 238000006136 alcoholysis reaction Methods 0.000 abstract 1
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
- 238000005267 amalgamation Methods 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- VHEKNAPNQRKGIM-UHFFFAOYSA-N benzyl-(ethoxymethyl)-dimethylsilane Chemical compound C(C)OC[Si](CC1=CC=CC=C1)(C)C VHEKNAPNQRKGIM-UHFFFAOYSA-N 0.000 abstract 1
- ABHNFDUSOVXXOA-UHFFFAOYSA-N benzyl-chloro-dimethylsilane Chemical compound C[Si](C)(Cl)CC1=CC=CC=C1 ABHNFDUSOVXXOA-UHFFFAOYSA-N 0.000 abstract 1
- TVRFAOJPBXYIRM-UHFFFAOYSA-N bis(chloromethyl)-dimethylsilane Chemical compound ClC[Si](C)(C)CCl TVRFAOJPBXYIRM-UHFFFAOYSA-N 0.000 abstract 1
- VTSILAHGPSRWNO-UHFFFAOYSA-N bis(chloromethyl)-methyl-propylsilane Chemical compound CCC[Si](C)(CCl)CCl VTSILAHGPSRWNO-UHFFFAOYSA-N 0.000 abstract 1
- XZUJPPOGIIKKLJ-UHFFFAOYSA-N bis(ethoxymethyl)-dimethylsilane Chemical compound [H]C([H])C([H])OC([H])([H])[Si](C([H])([H])[H])(C([H])([H])[H])C([H])([H])OC([H])C([H])[H] XZUJPPOGIIKKLJ-UHFFFAOYSA-N 0.000 abstract 1
- AEIQWKOGFRNHPY-UHFFFAOYSA-N bis(ethoxymethyl)-methylsilane Chemical compound C(C)OC[SiH](C)COCC AEIQWKOGFRNHPY-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- LADPCMZCENPFGV-UHFFFAOYSA-N chloromethoxymethylbenzene Chemical compound ClCOCC1=CC=CC=C1 LADPCMZCENPFGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- KTQYJQFGNYHXMB-UHFFFAOYSA-N dichloro(methyl)silicon Chemical compound C[Si](Cl)Cl KTQYJQFGNYHXMB-UHFFFAOYSA-N 0.000 abstract 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 abstract 1
- QTEHXUMWHSECQG-UHFFFAOYSA-N diphenyl-bis(phenylmethoxymethyl)silane Chemical compound C(C1=CC=CC=C1)OC[Si](C1=CC=CC=C1)(C1=CC=CC=C1)COCC1=CC=CC=C1 QTEHXUMWHSECQG-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000005055 methyl trichlorosilane Substances 0.000 abstract 1
- 239000005048 methyldichlorosilane Substances 0.000 abstract 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 235000010755 mineral Nutrition 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 235000011056 potassium acetate Nutrition 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- UIDUKLCLJMXFEO-UHFFFAOYSA-N propylsilane Chemical compound CCC[SiH3] UIDUKLCLJMXFEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 239000012266 salt solution Substances 0.000 abstract 1
- 229910000077 silane Inorganic materials 0.000 abstract 1
- UOULCEYHQNCFFH-UHFFFAOYSA-M sodium;hydroxymethanesulfonate Chemical compound [Na+].OCS([O-])(=O)=O UOULCEYHQNCFFH-UHFFFAOYSA-M 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- SIPHWXREAZVVNS-UHFFFAOYSA-N trichloro(cyclohexyl)silane Chemical compound Cl[Si](Cl)(Cl)C1CCCCC1 SIPHWXREAZVVNS-UHFFFAOYSA-N 0.000 abstract 1
- DOEHJNBEOVLHGL-UHFFFAOYSA-N trichloro(propyl)silane Chemical compound CCC[Si](Cl)(Cl)Cl DOEHJNBEOVLHGL-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/0825—Preparations of compounds not comprising Si-Si or Si-cyano linkages
- C07F7/083—Syntheses without formation of a Si-C bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR868789A FR1303195A (fr) | 1961-07-24 | 1961-07-24 | Procédé de préparation d'organosilanes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB971569A true GB971569A (en) | 1964-09-30 |
Family
ID=8759902
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2832262A Expired GB971569A (en) | 1961-07-24 | 1962-07-23 | Improvements in or relating to organosilanes and their preparation |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE620518A (ru) |
| FR (1) | FR1303195A (ru) |
| GB (1) | GB971569A (ru) |
| NL (1) | NL281317A (ru) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012140700A (ja) * | 2010-12-15 | 2012-07-26 | Tosoh Corp | 炭素含有酸化ケイ素膜、封止膜及びその用途 |
-
0
- NL NL281317D patent/NL281317A/xx unknown
- BE BE620518D patent/BE620518A/xx unknown
-
1961
- 1961-07-24 FR FR868789A patent/FR1303195A/fr not_active Expired
-
1962
- 1962-07-23 GB GB2832262A patent/GB971569A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012140700A (ja) * | 2010-12-15 | 2012-07-26 | Tosoh Corp | 炭素含有酸化ケイ素膜、封止膜及びその用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| NL281317A (ru) | |
| FR1303195A (fr) | 1962-09-07 |
| BE620518A (ru) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002179684A (ja) | オルガノシランの製造方法 | |
| GB795772A (en) | Organosilanes | |
| CA2019691C (en) | Preparation of tertiary-hydrocarbylsilyl compounds | |
| GB684310A (en) | Improvements in or relating to organosilicon carboxy esters | |
| Spialter et al. | The oxidative cleavage of organosilanes. III. Ozone and the silicon-alkyl,-aryl,-hydrogen, and-oxygen bonds | |
| GB971569A (en) | Improvements in or relating to organosilanes and their preparation | |
| GB692669A (en) | Improvements in or relating to organosilyl alcohols | |
| Westermark et al. | Preparation of some organic silicon hydrides | |
| US2582568A (en) | Silicon-containing esters | |
| GB1460699A (en) | Method of preparing fluoroalkyl-containing organosilanes | |
| US6156918A (en) | Process for the preparation of silanes, with a tertiary hydrocarbon group in the a-position relative to the silicon atom | |
| Tour et al. | Convenient route to di-and triorganosilyl ethyl ethers and the corresponding di-and triorganosilanes | |
| JPH06157554A (ja) | トリオルガノクロロシランの製造方法 | |
| JPH0786117B2 (ja) | アルコキシシラン | |
| GB1003948A (en) | A process for preparing organosilicon compounds | |
| Yogo et al. | Preparation of 1-Alkynyl (Trimethyl) Silanes from Trimethylsilylpropargyl Phenyl Ether and Organoboranes | |
| US2645644A (en) | Thienyl halosilanes | |
| FRISCH et al. | CYANOALKOXYSILANES | |
| JPS63253090A (ja) | トリメチルシロキシ基含有シリル（メタ）アクリレ−ト | |
| JPH06107671A (ja) | 有機ケイ素化合物及びその製造方法 | |
| KR20090041242A (ko) | 시클로알케닐실란폴리올 유도체와 이의 제조방법 | |
| SU447395A1 (ru) | Способ получени 3-замещенных 2,4, 10-триокса-3-силаадамантанов | |
| JPS606357B2 (ja) | モノハイドロジエンオルガノポリシロキサンの製造方法 | |
| GB740991A (en) | Improvements in and relating to hydrolyzable organosilylethynes | |
| GB900123A (en) | Improvements in or relating to the production of alkyl-or aryl-halosilanes |