反应详情

A solution of (R)-2-(5-bromo-2-fluoro-phenyl)-2-(4-methoxy-benzylamino)-propan-1-ol (6.95 g, 18.9 mmol) in dichloromethane (170 ml) was treated at room temperature with triethylamine (5.78 ml, 41.5 mmol), 4-dimethylaminopyridine (1.15 g, 9.43 mmol), and tert-butyldimethylchlorosilane (1.15 g, 37.7 mmol). After 16 hours at room temperature the reaction mixture was consecutively extracted with saturated sodium hydrogen-carbonate solution (100 ml), water (100 ml), and brine (100 ml). The aqueous layers were re-extracted with dichloromethane (100 ml). The combined organic layers were dried over sodium sulfate and evaporated at reduced pressure. After chromatography on Silicycle-Si-amine column using heptane as the eluent, [(R)-1-(5-bromo-2-fluoro-phenyl)-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-(4-methoxy-benzyl)-amine was obtained as a colorless oil (8.0 g, 88% of theory). Mass (calculated) C23H33BrFNO2Si [482.51]; (found) [M+H]+=482, [M+2-H]+=484.

1. extractionAfter 16 hours at room temperature the reaction mixture was consecutively extracted with saturated sodium hydrogen-carbonate solution (100 ml), water (100 ml), and brine (100 ml)
2. extractionThe aqueous layers were re-extracted with dichloromethane (100 ml)
3. dry with materialThe combined organic layers were dried over sodium sulfate
4. customevaporated at reduced pressure