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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

2-Methylenebutyrolactones. II. Fluorene and diaryl derivatives

LK Dalton, BC Elmes and BV Kolczynski

Australian Journal of Chemistry 25(3) 633 - 638
Published: 1972

Abstract

Ethyl sodiomalonate with fluorene-9-spiro-2'-oxiran gave two carboxybutyro-lactones, (2a) and (3a). Fluorene-9-spiro-4'-(2'-methylenebutyrolactone) (3c) and 2-methylene-4,4-diphenylbutyrolactone (6c) have been prepared by the action of diethylamine and formaldehyde on their respective 2-oarboxybutyrolaotones. The reaction of trimethylsulphonium iodide with 4,4'-diethoxybenzophenone gave 2,2-bis(4'-ethoxypheny1)vinyl alcohol (6a) and not the oxiran.

https://doi.org/10.1071/CH9720633

© CSIRO 1972

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