Bulletin of the Chemical Society of Japan p. 1667 - 1668 (1982)
Update date:2022-08-28
Topics:
Matsumura, Noboru
Matsukawa, Kimihiro
Sakaguchi, Yujiro
Inoue, Hiroo
It is found that 1-methoxycarbonyl- or 1-phenoxycarbonyl-2-imidazolidone reacts with phenylmagnesium bromide to afford benzophenone and triphenylmethanol, together with 2-imidazolidone, by nucleophilic attack on the carbonyl group at the side chain.
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