反应详情

50 g (270.2 mmol) 4-bromobenzaldehyde were dissolved in 200 ml of 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 sodium hydrogen carbonate-solution (2×) and water. The combined aqueous layers were extracted with Toluene and the combined organic layers were dried over magnesium sulfate and evaporated. The residue was dissolved in 200 ml of ethanol and 5.11 g (135.1 mmol) of 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 water. After drying over magnesium sulfate and evaporation, 60.5 g of the title compound were obtained (crude product), 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 sodium hydrogen carbonate-solution (2×) and water
4. extractionThe combined aqueous layers were extracted with Toluene
5. dry with materialthe combined organic layers were dried over magnesium sulfate
6. customevaporated
7. dissolutionThe residue was dissolved in 200 ml of ethanol
8. waitstanding overnight
9. customthe solvent was removed i
10. washwashed (2×) with water
11. dry with materialAfter drying over magnesium sulfate and evaporation