DE976684C - Process for the preparation of monomeric organosilicon compounds - Google Patents

Process for the preparation of monomeric organosilicon compounds

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Publication number
DE976684C
DE976684C DEK26023A DEK0026023A DE976684C DE 976684 C DE976684 C DE 976684C DE K26023 A DEK26023 A DE K26023A DE K0026023 A DEK0026023 A DE K0026023A DE 976684 C DE976684 C DE 976684C
Authority
DE
Germany
Prior art keywords
organosilicon compounds
preparation
monomeric organosilicon
monomeric
compounds
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
DEK26023A
Other languages
German (de)
Inventor
Herbert Dr Jenkner
Hans Werner Dr Schmidt
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
Priority to DEK26023A priority Critical patent/DE976684C/en
Application granted granted Critical
Publication of DE976684C publication Critical patent/DE976684C/en
Expired legal-status Critical Current

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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
    • 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

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

Description

Verfahren zur Herstellung von monomeren Organosiliciumverbindungen Nach dem Verfahren des älteren Patents 972 855 kann man monomere Organosiliciumverbindungen dadurch herstellen, daß man Silicium und Fluor enthaltende Verbindungen, bei denen das Fluor an Silicium gebunden ist, mit Aluminiumtrialkylen bei erhöhter Temperatur, vorzugsweise bei etwa. 200 bis 300° C. umsetzt.Process for the preparation of monomeric organosilicon compounds To The method of the earlier patent 972,855 can be used to produce monomeric organosilicon compounds by preparing silicon and fluorine-containing compounds in which the fluorine is bonded to silicon, with aluminum trialkyls at elevated temperature, preferably at about. 200 to 300 ° C.

Demgegenüber wurde gefunden, daß man monomere Organosiliciumverbindungen auch herstellen kann, indem man Salze der Kieselfluorwasserstoffwäure mit Organoaluminiumverbindungen der allgemeinen Formel RnAlF3-n, worin R eine Alkyl-oder Arylgruppe und/1 = i oder 2 bedeutet, bei erhöhter Temperatur, vorzugsweise bei etwa 200 bis 300°C, umsetzt. In contrast, it has been found that monomeric organosilicon compounds can also be prepared by adding salts of hydrofluoric acid with organoaluminum compounds of the general formula RnAlF3-n, where R is an alkyl or aryl group and / 1 = i or 2 means, at elevated temperature, preferably at about 200 to 300 ° C, is reacted.

Verschieden stark alkylierte Siliciumverhindungen können je nach dem Mischungsverhältnis von n Alkylaluminiumfluorid zu den Salzen der Kieselfluorwasserstoffsäure entstehen. Different strongly alkylated silicon compounds can depending on the mixing ratio of n alkyl aluminum fluoride to the salts of silicofluoric acid develop.

Die Reaktion kann auch unter Druck erfolgen. The reaction can also take place under pressure.

Beispiel i 104. Teile Diäthylaluminiumfluorid wurden mit W8 Teilen Natriumsilicofluorid im MIbad bis auf 225°C erhitzt. Bei dieser Temperatur bildeten sich in exothermer Rektion Äthylfluorislane und Tetraäthylsilan. Die einzelnen Verbindungen wurden nach Destillation in folgender prozentualer Zusammensetzung erhalten: 15% Si(C2H5)F3, 45% Si(C2H5)2F3, 15% Si(C2H5)3F, 25% Si(C2H5)4. Example i 104. parts of diethylaluminum fluoride were mixed with W8 parts Sodium silicofluoride in the MIbath except for Heated to 225 ° C. At this Temperature, ethyl fluoroislane and tetraethylsilane formed in an exothermic reaction. The individual compounds were in the following percentage composition after distillation obtained: 15% Si (C2H5) F3, 45% Si (C2H5) 2F3, 15% Si (C2H5) 3F, 25% Si (C2H5) 4.

Die Umsetzung, bezogen auf eingesetztes Diäthylaluminiumfluorid, war quantitativ. The implementation, based on the diethylaluminum fluoride used, was quantitative.

B e i s p i e l 2 I88 Teile Äthylaluminiumdifluorid wurden mit ige Teilen Natriumsilicofluorid bis auf 300° C erhitzt. Es wurden erhalten: 40% Si(C2H5)F3. 35% Si(C2H5)2F2, Rest Si(C2H5)3F und Si(C2H5)4. B e i s p i e l 2 188 parts of ethylaluminum difluoride were mixed with ige Parts of sodium silicofluoride heated up to 300 ° C. The following were obtained: 40% Si (C2H5) F3. 35% Si (C2H5) 2F2, remainder Si (C2H5) 3F and Si (C2H5) 4.

Claims (1)

PATENTANSPRUCH : Verfahren zur Herstellung von monomeren Organosillicumverbindunge, dadruch gekennzeichnet, daß man Salze der Kieselfluorwasserstoffsäure mit Organoaluminiumfluoriden der allgemienen Formel RnAlF3-n, woirn R eine Akyl- oder Arylgruppe und n = I oder 2 bedeutet, bei erhöhter Temperatur, vorzugsweise bei etwa 200 bis 300° C, umsetzt. PATENT CLAIM: Process for the production of monomeric organosilicate compounds, characterized by the fact that salts of silicofluoric acid with organoaluminum fluorides of the general formula RnAlF3-n, where R is an alkyl or aryl group and n = I or 2 means, at elevated temperature, preferably at about 200 to 300 ° C, is reacted. In Betracht gezogene Druckschriften : Deutsche Patentschriften Nr. 882 853, 908 019. Publications considered: German Patent Specifications No. 882 853, 908 019.
DEK26023A 1954-08-28 1954-08-28 Process for the preparation of monomeric organosilicon compounds Expired DE976684C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEK26023A DE976684C (en) 1954-08-28 1954-08-28 Process for the preparation of monomeric organosilicon compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEK26023A DE976684C (en) 1954-08-28 1954-08-28 Process for the preparation of monomeric organosilicon compounds

Publications (1)

Publication Number Publication Date
DE976684C true DE976684C (en) 1964-02-20

Family

ID=7217489

Family Applications (1)

Application Number Title Priority Date Filing Date
DEK26023A Expired DE976684C (en) 1954-08-28 1954-08-28 Process for the preparation of monomeric organosilicon compounds

Country Status (1)

Country Link
DE (1) DE976684C (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE882852C (en) * 1942-11-27 1953-07-13 Ciba Geigy Process for the production of condensation products
DE908019C (en) * 1950-06-09 1954-04-01 Bayer Ag Process for the preparation of alkyl and aryl halosilanes

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE882852C (en) * 1942-11-27 1953-07-13 Ciba Geigy Process for the production of condensation products
DE908019C (en) * 1950-06-09 1954-04-01 Bayer Ag Process for the preparation of alkyl and aryl halosilanes

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