Chloroacetamide → 2-Aminocarbonylmethoxyimino-2-(fur-2-yl)acetic acid

反応式

CC(C)([O-])C.[K+].[OH:7][N:8]=[C:9]([C:13]1[O:14][CH:15]=[CH:16][CH:17]=1)[C:10]([OH:12])=[O:11].Cl[CH2:19][C:20]([NH2:22])=[O:21]>CS(C)=O>[NH2:22][C:20]([CH2:19][O:7][N:8]=[C:9]([C:13]1[O:14][CH:15]=[CH:16][CH:17]=1)[C:10]([OH:12])=[O:11])=[O:21]

参加物

実験手順

To a solution of potassium t-butoxide (2.24 g) in dimethylsulphoxide (10 ml) was added a solution of 2-hydroxyimino-2-(fur-2-yl)acetic acid (syn isomer) (1.551 g) in dimethylsulphoxide (10 ml). The mixture was stirred for 30 minutes and a solution of chloroacetamide (0.935 g) in dimethylsulphoxide (10 ml) was added. The mixture was stirred for a further 2 hours, when a clear solution had formed. This solution was poured into ice-water (50 ml) and the mixture was extracted with ethyl acetate. The layers were separated and the aqueous layer was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extracts were washed with brine and dried, and the solvent was evaporated. The resulting yellow oil was triturated with dichloromethane to give the title compound (0.51 g, 24%), m.p. 143°-145°; λ max (EtOH) 275nm (ε 14,100).