Sodium Hydroxide → 4-(3,4-Dichlorobenzyl)thieno[3,2-b]pyrrole-5-carboxylic acid

反応式

[OH-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]([CH:21]=[CH:22][C:23]=1[Cl:24])[CH2:7][N:8]1[C:12]([C:13]([O:15]CC)=[O:14])=[CH:11][C:10]2[S:18][CH:19]=[CH:20][C:9]1=2>C1COCC1.CO>[Cl:3][C:4]1[CH:5]=[C:6]([CH:21]=[CH:22][C:23]=1[Cl:24])[CH2:7][N:8]1[C:12]([C:13]([OH:15])=[O:14])=[CH:11][C:10]2[S:18][CH:19]=[CH:20][C:9]1=2

参加物

実験手順

Sodium hydroxide (3N, 1.3 ml) was added to a stirred solution of ethyl 4-(3,4-dichlorobenzyl)thieno[3,2-b]pyrrole-5-carboxylate (0.137 g) in THF (2.5 ml) and methanol (2.5 ml). Stirring was continued for 16 hours at ambient temperature, concentrated in vacuo and the residue dissolved in water. Dropwise addition of acetic acid led to precipitation of the product as a white solid which was filtered and dried (0.107 g, 85%), NMR d(DMSO) 5.79 (2H, s), 7.05 (1H, m), 7.28 (2H, m), 7.42 (1H, s), 7.60 (2H, m); M/z (−) 326 (M+), 324, 282, 280.