tert-Butoxy bis(dimethylamino)methane → 5-Dimethylaminomethylene-4-oxo-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxylic acid tert-butyl ester
反応式
[C:1]([O:5][C:6]([C:8]1[S:12][C:11]2[CH2:13][CH2:14][CH2:15][C:16](=[O:17])[C:10]=2[CH:9]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CC(O[CH:23](N(C)C)[N:24]([CH3:26])[CH3:25])(C)C>C1(C)C=CC=CC=1>[C:1]([O:5][C:6]([C:8]1[S:12][C:11]2[CH2:13][CH2:14][C:15](=[CH:23][N:24]([CH3:26])[CH3:25])[C:16](=[O:17])[C:10]=2[CH:9]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]参加物
4
実験手順
4-Oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-2-carboxylic acid tert-butyl ester (8.75 g, 34.68 mmol) was suspended in dry toluene (40 mL) and Bredereck's reagent (6.65 g, 38.14 mmol) was added. The resulting suspension was heated at reflux for 2 hours, during which time all starting material dissolved, allowed to cool to room temperature and concentrated under reduced pressure. The resulting oil was purified by silica gel chromatography (50% EtOAc in hexanes on 1 L silica, loaded as a solution in dichloromethane) to afford the title compound as a brown solid (6.21 g, 58% yield). MS (ES+) 308. δH (CDCl3) 1.5-1.6 (9H, s), 2.9-3.0 (2H, m), 3.0-3.1 (2H, m), 3.1 (6H, s), 7.6 (1H, s), 8.0 (1H, s).