PROPARGYL ETHERS OF PHENOL
CD Hurd, FL Cohen
Index: Hurd; Cohen Journal of the American Chemical Society, 1931 , vol. 53, p. 1073
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Citation Number: 11
Abstract
The yield was about 45%. This reaction is similar evidently to the pyrolysis of triphenylmethyl chloride, wherein hydrogen chloride was detached at temperatures above 200'and 9- phenylfluorene formed. Similar also is the production of phenyl-a-naphthofluorene by refluxing diphenyla-naphthylchloromethane6 with zinc chloride in acetic acid.
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