4,6-Dimethoxysalicylaldehyde → 3-(4-Methoxybenzylsulfonyl)-5,7-dimethoxy-2H-chromen-2-one
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5](O)[C:6](=[C:9]([O:11][CH3:12])[CH:10]=1)[CH:7]=O.[CH3:14][O:15][C:16]1[CH:29]=[CH:28][C:19]([CH2:20][S:21]([CH2:24][C:25]([OH:27])=[O:26])(=[O:23])=[O:22])=[CH:18][CH:17]=1>C(O)(=O)C>[CH3:14][O:15][C:16]1[CH:17]=[CH:18][C:19]([CH2:20][S:21]([C:24]2[C:25](=[O:27])[O:26][C:5]3[C:6]([CH:7]=2)=[C:9]([O:11][CH3:12])[CH:10]=[C:3]([O:2][CH3:1])[CH:4]=3)(=[O:22])=[O:23])=[CH:28][CH:29]=1参加物
4
実験手順
A solution of 4,6-dimethoxysalicylaldehyde (1 mmol) and 2-(4-methoxybenzylsulfonyl)acetic acid (1 mmol) in acetic acid (10 mL) was subjected to the General Procedure 2, Method A to generate a 58% yield of the title compound; m.p. 183-185° C.