反应详情

50 g (270.2 mmol) 4-bromobenzaldehyde were dissolved in 200 ml toluene and 28.4 g (270.2 mmol) aminoacetaldehyde dimethylacetal were added. After the addition of 5.1 g (27.0 mmol) p-toluenesulfonic acid monohydrate, the reaction mixture was heated under reflux in a Dean Stark apparatus. After 4 h, the reaction was cooled to room temperature and washed with saturated NaHCO3-solution (2×) and H2O. The combined aqueous layers were extracted with toluene and the combined organic layers were dried with MgSO4 and evaporated. The residue was dissolved in 200 ml ethanol and 5.11 g (135.1 mmol) sodium borohydride were added in small portions. After stirring for 2 h at room temperature and standing overnight, 5.0 ml acetic acid were added and the solvent was removed i. vac. The residue was taken up in dichloromethane and washed (2×) with H2O. After drying with MgSO4 and evaporation, 60.5 g of the title compound were obtained, which were used without further purification. Rt=0.80 min (Method C). Detected mass: 274.1/276.1 (M+H+).

1. temperaturethe reaction mixture was heated
2. temperatureunder reflux in a Dean Stark apparatus
3. washwashed with saturated NaHCO3-solution (2×) and H2O
4. extractionThe combined aqueous layers were extracted with toluene
5. dry with materialthe combined organic layers were dried with MgSO4
6. customevaporated
7. dissolutionThe residue was dissolved in 200 ml ethanol
8. waitstanding overnight
9. customthe solvent was removed i
10. washwashed (2×) with H2O
11. dry with materialAfter drying with MgSO4 and evaporation