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A-AMINOBENZYL CYANIDE

Aminobenzyl alcohol, 21,10 a-AMINOBENZYL CYANIDE, 22, 23, 25 2-Amino- -cymene, 22, 9 < -AMINODIETHYLACETIC ACID, 22, 13 a-AMINO-a-ETHYLBUTYRIC ACID, 22, 13 2-Aminoheptane, 23, 70 (Z/-0-AMINOHYDROCINNAMIC ACID, 22, 26 a-AMINOISOVALERIC ACID, 20, 106... [Pg.55]

Nitrile see a-Aminobenzyl cyanide. N-Formyl dates from HgO, needles from EtOH. M.p. 190° decomp. 259-9° in EtOH. [Pg.118]

Type C Syntheses (C—C—N—C + S).—The reaction of a-aminobenzyl cyanide, PhCH(NHa)CN, with aldehydes and sulphur in the presence of an organic base results in good yields of anils (9), which are hydrolysed by acids to 2-substituted... [Pg.358]

Aminobenzonitrile is prepared by reduction of 3-nitrobenzonitrile by sodium disulfide in aqueous suspension (63%). This reagent causes some hydrolysis of the cyano group. A selective hydrogenation of the more reactive nitro group in the presence of the cyano group can also be done, e.g., in the preparation of p-aminobenzyl cyanide (7S>%). ... [Pg.780]

See other pages where A-AMINOBENZYL CYANIDE is mentioned: [Pg.278]    [Pg.118]    [Pg.278]    [Pg.118]   
See also in sourсe #XX -- [ Pg.22 , Pg.23 , Pg.25 ]

See also in sourсe #XX -- [ Pg.22 , Pg.23 , Pg.25 ]

See also in sourсe #XX -- [ Pg.22 , Pg.23 , Pg.25 ]

See also in sourсe #XX -- [ Pg.22 , Pg.23 , Pg.25 ]



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2-Aminobenzyl cyanide

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