GB869962A - Method of purifying diorganodihalogenosilanes - Google Patents
Method of purifying diorganodihalogenosilanesInfo
- Publication number
- GB869962A GB869962A GB33049/58A GB3304958A GB869962A GB 869962 A GB869962 A GB 869962A GB 33049/58 A GB33049/58 A GB 33049/58A GB 3304958 A GB3304958 A GB 3304958A GB 869962 A GB869962 A GB 869962A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- ether
- trichlorosilane
- dichlorosilane
- silanes
- 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 abstract 3
- 239000005052 trichlorosilane Substances 0.000 abstract 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000004756 silanes Chemical class 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 229910000077 silane Inorganic materials 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-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
- C07F7/20—Purification, separation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
A diorganodichlorosilane of greater purity is obtained from mixtures of such silane and an organotrichlorosilane in which the trichlorosilane comprises at most 20% by weight of the mixture by adding a solution of water and an ether miscible with both the water and silanes, the amount of water being substantially less than that required to hydrolyse the dichlorosilane and being from 0,5 to 2 moles per mole of the trichlorosilane, and recovering the dichlorosilane, e.g., by distillation. The ether, which effects a preferential hydrolysis of the trichlorosilane, is preferably in an amount of 2 to 50 moles per mole of water. Specified ethers are dioxane, tetrahydrofuran, diethyl ether and dipropyl ether. Reaction may be carried out at room temperatures or up to 150 DEG C. The organic radicals on the silanes may be alkyl, alicyclic, aryl, alkaryl, aralkyl and alkenyl, and they may be substituted, e.g., by halogen, cyano and amino groups. Specification 712,059 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US869962XA | 1957-11-18 | 1957-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB869962A true GB869962A (en) | 1961-06-07 |
Family
ID=22202206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB33049/58A Expired GB869962A (en) | 1957-11-18 | 1958-10-16 | Method of purifying diorganodihalogenosilanes |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1085157B (en) |
FR (1) | FR1215336A (en) |
GB (1) | GB869962A (en) |
-
1958
- 1958-10-16 GB GB33049/58A patent/GB869962A/en not_active Expired
- 1958-11-14 DE DEG25711A patent/DE1085157B/en active Pending
- 1958-11-18 FR FR779404A patent/FR1215336A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1215336A (en) | 1960-04-15 |
DE1085157B (en) | 1960-07-14 |
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