The Preparation of Some Mono-and Dialkylcyclohexanes

FK Signaigo, PL Cramer

Index: Signaigo; Cramer Journal of the American Chemical Society, 1933 , vol. 55, p. 3326,3330

Full Text: HTML

Citation Number: 44

Abstract

Summary A synthesis of camphor from bornyl chloride, passing through isobornylaniline and camphor: mil, has been described. The yield of camphor from bornyl chloride by this procedure is 89%. The action of nickel catalysts on isobornylaniline has been found to result, according to the conditions, in camphor anil, or a mixture of camphene and aniline.

Related Articles:

Syntheses with Dihydroresorcinol Mono Ethyl Ether: 3-Alkyl-Δ2-cyclohexenones

[Woods et al. Journal of the American Chemical Society, 1949 , vol. 71, p. 2028]

Syntheses with Dihydroresorcinol Mono Ethyl Ether: 3-Alkyl-Δ2-cyclohexenones

[Woods et al. Journal of the American Chemical Society, 1949 , vol. 71, p. 2028]

Δ2-cyclohexenone and related substances

[Whitmore; Pedlow Journal of the American Chemical Society, 1941 , vol. 63, p. 758]

Δ2-cyclohexenone and related substances

[Whitmore; Pedlow Journal of the American Chemical Society, 1941 , vol. 63, p. 758]

More Articles...