反应详情

温度

70 °C

Trimethoxy borane (2.0 g) was added at room temperature to a stirred solution of (S)-diphenylprolinol (3.5 g) in toluene (100 mL). After stirring this mixture for 90 minutes at about 65-75° C., borane dimethylsulfide (2M THF solution, 105 mL) was added over a period of 50 minutes maintaining the temperature between 65 and 75° C. This mixture was stirred for another 90 minutes at 75° C., then a solution of 2-chloro-1-(3,4-difluorophenyl)ethanone (50.0 g) in toluene (150 mL) was dosed over a period of 25 minutes maintaining the temperature between 65 and 75° C. After the completion of the addition the reaction mixture was stirred for another 100 minutes at 75° C. at which point the completion of reaction was monitored by TLC. Then mixture was cooled to 0-5° C. and methanol (50 mL) was added over a period of 30 minutes controlling the gas formation and the temperature to a maximum of 5° C. After the addition is complete, the obtained solution was subjected to distillation under reduced pressure at below 60° C., followed by sequential addition of 10% aqueous acetic acid solution (250 mL) and toluene (500 mL) to the residue. The layers were separated and obtained water layer was back extracted with toluene (250 mL). Both organic layers were combined and washed with water (500 mL). The resulting organic layer was subjected to complete distillation under vacuum to afford the title compound in 94.2% yield having chiral HPLC purity of 99.62%.

1. temperaturemaintaining the temperature between 65 and 75° C
2. stirringThis mixture was stirred for another 90 minutes at 75° C.
3. temperaturemaintaining the temperature between 65 and 75° C
4. additionAfter the completion of the addition the reaction mixture
5. stirringwas stirred for another 100 minutes at 75° C. at which point
6. customthe completion of reaction
7. temperatureThen mixture was cooled to 0-5° C.
8. customto a maximum of 5° C
9. additionAfter the addition
10. distillationthe obtained solution was subjected to distillation under reduced pressure at below 60° C.
11. additionfollowed by sequential addition of 10% aqueous acetic acid solution (250 mL) and toluene (500 mL) to the residue
12. customThe layers were separated
13. customobtained water layer
14. extractionwas back extracted with toluene (250 mL)
15. washwashed with water (500 mL)
16. distillationThe resulting organic layer was subjected to complete distillation under vacuum