The Synthesis of 3-(3-Cyclohexylpropyl)-4-quinolinol1

RH Baker, RM Dodson

Index: Baker; Dodson Journal of the American Chemical Society, 1946 , vol. 68, p. 1283

Full Text: HTML

Citation Number: 5

Abstract

Summary 3-Dibutylaminomethyl-7-methoxy-2-methyl-4-quinolinol has been prepared by the action of formaldehyde and dibutylamine upon 7-methoxy-2-methyl-4-quinolino1. Its structure follows from its hydrogenolysis to 2, 3-dimethyl-7-methoxy-4-quinolinol, which was identical with samples prepared by two alternative methods.

Related Articles:

Preparation, structure, and reactivity of nonstabilized organoiron compounds. Implications for iron-catalyzed cross coupling reactions

[Fuerstner, Alois; Martin, Ruben; Krause, Helga; Seidel, Guenter; Goddard, Richard; Lehmann, Christian W. Journal of the American Chemical Society, 2008 , vol. 130, # 27 p. 8773 - 8787]

Organic carbonates as solvents in synthesis and catalysis

[Curran, Dennis P.; Zhang, Qisheng Advanced Synthesis and Catalysis, 2003 , vol. 345, # 3 p. 329 - 332]

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]

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]

C–C bond formation from alcohols and malonate half esters using borrowing hydrogen methodology

[Pridmore, Simon J.; Williams, Jonathan M.J. Tetrahedron Letters, 2008 , vol. 49, # 52 p. 7413 - 7415]

More Articles...