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O Carboxybenzyl cyanide

The heating of lactones with powdered alkali cyanides leads to salts of cyano acids. The procedure is illustrated (above equation) by the synthesis of o-carboxybenzyl cyanide from phthalide and potassium cyanide (67-83%). In another instance, the reaction of potassium Cyanide with y-anisyl-y-butyrolactone involves a rearrangement thereby forming a /3-cyano acid instead of the anticipated y-cyano acid, ... [Pg.309]

Carbostyril, 4-methyi, 24, 68 Carboxyaldehyde, 23, 76 o-Carboxybenzyl cyanide, 22,30 o-Carboxyphenylacetonitrile, 22,... [Pg.53]

See other pages where O Carboxybenzyl cyanide is mentioned: [Pg.101]    [Pg.53]    [Pg.405]    [Pg.200]    [Pg.101]    [Pg.53]    [Pg.405]    [Pg.200]    [Pg.54]   
See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]

See also in sourсe #XX -- [ Pg.22 , Pg.30 ]



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