GB900132A - Method of producing alkyls - Google Patents

Method of producing alkyls

Info

Publication number
GB900132A
GB900132A GB35357/60A GB3535760A GB900132A GB 900132 A GB900132 A GB 900132A GB 35357/60 A GB35357/60 A GB 35357/60A GB 3535760 A GB3535760 A GB 3535760A GB 900132 A GB900132 A GB 900132A
Authority
GB
United Kingdom
Prior art keywords
alkyl
complex
alkali
aluminium compound
distilled
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
GB35357/60A
Inventor
Herbert Jenkner
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.)
Kali Chemie AG
Original Assignee
Kali Chemie AG
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
Application filed by Kali Chemie AG filed Critical Kali Chemie AG
Publication of GB900132A publication Critical patent/GB900132A/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
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/0825Preparations of compounds not comprising Si-Si or Si-cyano linkages
    • C07F7/0827Syntheses with formation of a Si-C bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F3/00Compounds containing elements of Groups 2 or 12 of the Periodic Table
    • C07F3/06Zinc compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/027Organoboranes and organoborohydrides
    • 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
    • C07F7/22Tin compounds
    • C07F7/2208Compounds having tin linked only to carbon, hydrogen and/or halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)

Abstract

Alkyls of silicon are made by reacting a halide, alkoxy or aryloxy compound of silicon with an alkali-metal tetraalkyl aluminium compound in such stoichiometric proportions that the complex aluminium compound yields only one of its alkyl groups. Halide compounds include those of formula SiX4-m Rm where R is hydrogen, alkyl, aryl or an unsaturated organic radical, and m is an integer between 1 and 3. The reaction may be carried out in an inert solvent, e.g. an aliphatic or aromatic hydrocarbon, a mineral or paraffin oil or the alkyl which is to be produced. The desired alkyl may be distilled from the reaction mixture, or if preferred, an alkali-metal hydride may be added to complex with the trialkyl aluminium produced, the desired alkyl distilled off and the complex hydride olefinated to the original alkali-metal tetraalkyl aluminium compound. In Example (3) SiCl4 is reacted with sodium tetraethylaluminium to give Si(C2H5)4.ALSO:Alkyls of boron, tin, zinc, mercury, arsenic, antimony and bismuth are made by reacting a halide, alkoxy or aryloxy compound of the element with an alkali-metal tetraalkyl aluminium compound in such stoichiometric proportions that the complex aluminium compound yields only one of its alkyl groups. Halide compounds include those of formula ElXn-mRm where El is the selected element, R is hydrogen, alkyl, aryl or an unsaturated organic radical, n is the valency of El and m is an integer between 1 and n-1. The reaction may be carried out in an inert solvent e.g. an aliphatic or aromatic hydrocarbon, a mineral or paraffin oil or the alkyl which is to be produced. The desired alkyl may be distilled from the reaction mixture, or if preferred, an alkali-metal hydride may be added to complex with the trialkyl aluminium produced, the desired alkyl distilled off and the complex hydride definated to the original alkali metal tetraalkyl aluminium compound.
GB35357/60A 1959-10-17 1960-10-14 Method of producing alkyls Expired GB900132A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEK38941A DE1153367B (en) 1959-10-17 1959-10-17 Process for the preparation of the alkyls of boron, silicon, zinc and tin

Publications (1)

Publication Number Publication Date
GB900132A true GB900132A (en) 1962-07-04

Family

ID=7221554

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35357/60A Expired GB900132A (en) 1959-10-17 1960-10-14 Method of producing alkyls

Country Status (2)

Country Link
DE (1) DE1153367B (en)
GB (1) GB900132A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3398171A (en) * 1964-03-02 1968-08-20 Ethyl Corp Process of producing organohalosilanes
US4711965A (en) * 1987-02-24 1987-12-08 Ethyl Corporation Preparation of alkyl silanes
US4711966A (en) * 1987-03-19 1987-12-08 Ethyl Corporation Preparation of alkyl silanes
US4845260A (en) * 1987-02-24 1989-07-04 Ethyl Corporation Preparation of alkyl silanes
US4916245A (en) * 1988-05-25 1990-04-10 Ethyl Corporation Preparation of alkyl silanes
US4973724A (en) * 1987-02-24 1990-11-27 Ethyl Corporation Preparation of alkyl silanes
US4999447A (en) * 1987-02-24 1991-03-12 Ethyl Corporation Preparation of alkyl silanes
EP0796859A1 (en) * 1996-03-19 1997-09-24 Witco GmbH Stable homogenous formulations of oxidation-sensitive organometallic compounds in paraffines and process for their preparation

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2859229A (en) * 1955-03-25 1958-11-04 Ethyl Corp Manufacture of organolead compounds

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3398171A (en) * 1964-03-02 1968-08-20 Ethyl Corp Process of producing organohalosilanes
US4711965A (en) * 1987-02-24 1987-12-08 Ethyl Corporation Preparation of alkyl silanes
US4845260A (en) * 1987-02-24 1989-07-04 Ethyl Corporation Preparation of alkyl silanes
US4973724A (en) * 1987-02-24 1990-11-27 Ethyl Corporation Preparation of alkyl silanes
US4999447A (en) * 1987-02-24 1991-03-12 Ethyl Corporation Preparation of alkyl silanes
US4711966A (en) * 1987-03-19 1987-12-08 Ethyl Corporation Preparation of alkyl silanes
US4916245A (en) * 1988-05-25 1990-04-10 Ethyl Corporation Preparation of alkyl silanes
EP0796859A1 (en) * 1996-03-19 1997-09-24 Witco GmbH Stable homogenous formulations of oxidation-sensitive organometallic compounds in paraffines and process for their preparation

Also Published As

Publication number Publication date
DE1153367B (en) 1963-08-29

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