反应详情

After dissolving the 1-[3-(tert-butyl)-4-methoxy-5-morpholinophenyl]-1-ethanone (76 g) in tetrahydrofuran (600 ml), triethylamine (110 ml) and tert-butyl dimethylsilyltrifluoromethanesulfonate (75 ml) was added dropwise while cooling on ice. The reaction mixture was stirred for 30 minutes while cooling on ice and then N-bromosuccinimide (70 g) was gradually added. After stirring the reaction mixture for 30 minutes, 2 l of ether was added and the mixture was washed twice with water. The organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (33.7 g) as light yellow crystals.

1. additionwas added dropwise
2. temperaturewhile cooling on ice
3. temperaturewhile cooling on ice
4. stirringAfter stirring the reaction mixture for 30 minutes
5. washthe mixture was washed twice with water
6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
7. distillationthe solvent was distilled off under reduced pressure
8. customthe residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate)