1948
DOI: 10.1021/cr60132a001
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The Preparation of Nitriles.

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Cited by 392 publications
(113 citation statements)
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“…[7] Synthesis of nitriles using the concept of green chemistry has been considered to be a great scientific challenge. [8] Usually synthesis of nitriles is accomplished by substitution reactions of alkyl and aryl halides with metal cyanides, [9] oxidation of primary amines, [10] dehydration of primary and secondary amides, [11] or dehydration of aldoximes with dehydrating agents. [12] Other reported methods for the synthesis of nitriles include a one-pot reaction of aldehydes and hydroxylammonium chloride using reagents such as I 2 =NH 3 =tetrahydrofuran (THF), [13] NaN 3 =AlCl 3 , [14] and dimethylsulfoxide (DMSO)-I 2 .…”
Section: Introductionmentioning
confidence: 99%
“…[7] Synthesis of nitriles using the concept of green chemistry has been considered to be a great scientific challenge. [8] Usually synthesis of nitriles is accomplished by substitution reactions of alkyl and aryl halides with metal cyanides, [9] oxidation of primary amines, [10] dehydration of primary and secondary amides, [11] or dehydration of aldoximes with dehydrating agents. [12] Other reported methods for the synthesis of nitriles include a one-pot reaction of aldehydes and hydroxylammonium chloride using reagents such as I 2 =NH 3 =tetrahydrofuran (THF), [13] NaN 3 =AlCl 3 , [14] and dimethylsulfoxide (DMSO)-I 2 .…”
Section: Introductionmentioning
confidence: 99%
“…3 Aryl nitriles have been prepared by cyanation of iodides or bromides using CuCN or KCN in absence of solvent or in solvents like pyridine, quinoline, DMF, NMP at elevated temperature. [4][5][6][7][8][9][10][11] Under Von Braun conditions the reaction of 5-bromo-2-methoxypyrimidine with [ 14 C] CuCN in DMF at 1451C for 48 h did not yield cyano derivative.…”
Section: Resultsmentioning
confidence: 99%
“…J. Chem. Downloaded from www.nrcresearchpress.com by 13 Murakoshi's work (6) has delineated the cyclization of o-acylaminocarboxylic acids to cyclic imines and iminium salts (6, 7). We repeated his work using the commercially available 22.…”
Section: Resultsmentioning
confidence: 99%