Issue 12, 1978

Dealkylation of chelating ethers by reaction with WCl4Y (Y = O, S, Se, or NC2Cl5)

Abstract

Cleavage of an alkyl-oxygen bond occurs when WCl4Y (Y = O, S, Se, or NC2Cl5) reacts with ROCH2CH2OR (R = alkyl) or 1,2-dialkoxybenzene. The products of the reaction are an alkyl chloride and a tungsten alkoxide of the type [WCl3Y(OCH2CH2OR)] or [WCl3Y(OC6H4OR-2)]. The stages through which the reaction of MeOCH2CH2OMe with WCl4O passes have been fully investigated and the nature of the final product has been verified by the formation of a number of alkoxides of the type [WCl3O(OCH2CH2OR)] from the reaction of WCl4O with ROCH2CH2 OH.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1978, 1658-1661

Dealkylation of chelating ethers by reaction with WCl4Y (Y = O, S, Se, or NC2Cl5)

G. A. W. Fowles, D. A. Rice and K. J. Shanton, J. Chem. Soc., Dalton Trans., 1978, 1658 DOI: 10.1039/DT9780001658

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