A Convenient Method of Obtaining 2-Cyano-4-Alkylphenols, 4-Cyanophenol and 4-Cyanoaniline

…, R Dabrowski, J Dziabuszek

Index: Adamska; Dabrowski; Dziabuszek Molecular crystals and liquid crystals, 1981 , vol. 76, # 1-2 p. 93 - 99

Full Text: HTML

Citation Number: 7

Abstract

Abstract A convenient method is described of obtaining 2-cyano-4-alkylphenols and 4- cyanophenol by substituting bromine atom for the cyano group in the respective bromoanisoles and demethylation of the cyanoalkylanisoles. It is suggested to prepare 4- cyanoaniline by reduction of 4-cyano-nitrobenzene with aqueous hydrazine solutions.

Related Articles:

Suzuki–Miyaura cross-coupling of lithium n-alkylborates

[Zou, Gang; Falck Tetrahedron Letters, 2001 , vol. 42, # 34 p. 5817 - 5819]

Direct catalytic cross-coupling of organolithium compounds

[Giannerini, Massimo; Fananas-Mastral, Martin; Feringa, Ben L. Nature Chemistry, 2013 , vol. 5, # 8 p. 667 - 672]

Direct catalytic cross-coupling of organolithium compounds

[Giannerini, Massimo; Fananas-Mastral, Martin; Feringa, Ben L. Nature Chemistry, 2013 , vol. 5, # 8 p. 667 - 672]

Functional Group Tolerant Kumada− Corriu− Tamao Coupling of Nonactivated Alkyl Halides with Aryl and Heteroaryl Nucleophiles: Catalysis by a Nickel Pincer …

[Vechorkin, Oleg; Proust, Valerie; Hu, Xile Journal of the American Chemical Society, 2009 , vol. 131, # 28 p. 9756 - 9766]

One-step cross-coupling reaction of functionalized alkyl iodides with aryl halides by the use of an electrochemical method

[Kurono, Nobuhito; Sugita, Kazuya; Takasugi, Shingo; Tokuda, Masao Tetrahedron, 1999 , vol. 55, # 19 p. 6097 - 6108]

More Articles...