GB1336926A - Method of producing organochlorosilanes - Google Patents

Method of producing organochlorosilanes

Info

Publication number
GB1336926A
GB1336926A GB3116971A GB3116971A GB1336926A GB 1336926 A GB1336926 A GB 1336926A GB 3116971 A GB3116971 A GB 3116971A GB 3116971 A GB3116971 A GB 3116971A GB 1336926 A GB1336926 A GB 1336926A
Authority
GB
United Kingdom
Prior art keywords
benzene
bis
aryl
organochlorosilanes
chloroaryl
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
Application number
GB3116971A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Vainshtein B I
Original Assignee
Vainshtein B I
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from SU1447056A external-priority patent/SU316335A1/en
Application filed by Vainshtein B I filed Critical Vainshtein B I
Publication of GB1336926A publication Critical patent/GB1336926A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/12Organo silicon halides
    • C07F7/121Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20
    • C07F7/122Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20 by reactions involving the formation of Si-C linkages
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Silicon Polymers (AREA)

Abstract

1336926 Organochlorosilanes B I VAINSHTEIN A V ZIMIN E A CHERNYSHOV M E KUREK A N POLIVANOY L P BOGOVTSEVA E S STARODUBTSEV Z A I MASLJUKOV V I ANDREEV A E ZERETS and B I ZOROV 2 July 1971 [4 July 1970] 31169/71 Heading C3S Organochlorosilanes of the formulµ RR<SP>1</SP> n Si- Cl 3-n and R<SP>11</SP>(SiR<SP>1</SP> n Cl 3-n ) 2 , wherein R denotes aryl, chloroaryl, fluoroaryl, fluorochloroaryl, functionally-substituted aryl or a heterocyclic radical, R<SP>1</SP> deontes aryl or alkyl, R<SP>11</SP> denotes arylene, chloroarylene, fluoroarylene or functonally-substituted arylene, and n is 0, 1 or 2, are prepared by vapour phase reaction between hydrochlorosilanes of the formula HSiR<SP>1</SP> n Cl 3-n and chloroaryl compounds of the formula RCl or R<SP>11</SP>Cl 2 at temperatures not exceeding 450‹ C. and under the action of ionizing radiation. Atmospheric or elevated pressures may be employed. Suitable ionizing radiation includes gamma and beta radiation, and fast electron beams. Examples describe the preparation of phenyltrichlorosilane, methylphenyldichlorosilane, methyldichlorophenyldichlorosilane, ortho - trichlorosilyldiphenyl, meta - trifluoromethylphenyltrichlorosilane, 2 - trichlorosilylthiophene, ortho - trichlorosilylbenzonitrile, methylpentafluorophenyldichlorosilane, 1,4-bis- (trichlorosilyl)benzene, 1,4 - bis - (methyldichlorosilyl)benzene and 1,4-bis-(dimethylchlorosilyl)benzene. Other possible products are also specified. Uses.-The monomer products may be used to prepare resins, rubbers, cured rubbers and other organosilicon polymers.
GB3116971A 1970-07-04 1971-07-02 Method of producing organochlorosilanes Expired GB1336926A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1447056A SU316335A1 (en) 1970-07-04 Method of producing organochlorosilane

Publications (1)

Publication Number Publication Date
GB1336926A true GB1336926A (en) 1973-11-14

Family

ID=20453833

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3116971A Expired GB1336926A (en) 1970-07-04 1971-07-02 Method of producing organochlorosilanes

Country Status (4)

Country Link
DE (1) DE2132569C3 (en)
FR (1) FR2100122A5 (en)
GB (1) GB1336926A (en)
IT (1) IT941420B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI845161A0 (en) * 1984-12-28 1984-12-28 Ksv Chemicals Oy YTBEHANDLINGSMEDEL.
DE10349286A1 (en) 2003-10-23 2005-05-25 Wacker-Chemie Gmbh Production of organosilane, e.g. phenyltrichlorosilane, involves reacting a hydrogen-silane with a halogenated hydrocarbon in presence of a radical initiator of the alkane, diazene or disilane type, e.g. 1,2-diphenylethane

Also Published As

Publication number Publication date
FR2100122A5 (en) 1972-03-17
IT941420B (en) 1973-03-01
DE2132569B2 (en) 1974-10-31
DE2132569C3 (en) 1975-06-12
DE2132569A1 (en) 1972-02-10

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee