GB856857A - Method of producing boron trialkyls - Google Patents

Method of producing boron trialkyls

Info

Publication number
GB856857A
GB856857A GB20660/59A GB2066059A GB856857A GB 856857 A GB856857 A GB 856857A GB 20660/59 A GB20660/59 A GB 20660/59A GB 2066059 A GB2066059 A GB 2066059A GB 856857 A GB856857 A GB 856857A
Authority
GB
United Kingdom
Prior art keywords
boric acid
boron
activated
boron trioxide
trialkyls
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
GB20660/59A
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 GB856857A publication Critical patent/GB856857A/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
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic System
    • C07F5/02Boron compounds
    • C07F5/027Organoboranes and organoborohydrides

Abstract

Boron trialkyls are prepared by reacting boron trioxide, activated by the addition of boric acid esters, with aluminium trialkyls. Preferably the boron trioxide used is obtained by vacuum dehydration of boric acid at an elevated temperature. The boron trioxide may be activated with 10-90% mol of boric acid ester. Boric acid methyl ester is preferred but other esters up to and including the butyl ester may be used. The reaction proceeds at any temperature between 20 and 180 DEG C. and may be effected in the presence of solvents or diluents such as mineral oils and hydrocarbons, aromatic compounds and ethers. an example, boron trioxide activated with boric acid methyl ester is dissolved in diethylene glycol dimethyl ether and reacted with aluminium triethyl at 75 DEG C. to give boron triethyl.
GB20660/59A 1958-07-19 1959-06-16 Method of producing boron trialkyls Expired GB856857A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE856857X 1958-07-19

Publications (1)

Publication Number Publication Date
GB856857A true GB856857A (en) 1960-12-21

Family

ID=6789425

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20660/59A Expired GB856857A (en) 1958-07-19 1959-06-16 Method of producing boron trialkyls

Country Status (1)

Country Link
GB (1) GB856857A (en)

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