反应详情

A solution of 48.615 g (146.6 mmole) carbon tetrabromide in 150 mL methylene chloride was added dropwise with stirring to a solution of 76.895 g (293.2 mmole) triphenylphosphine in 150 mL methylene chloride in a 1-L rb flask with ice bath cooling over 1.75 h. After 40 minutes, a solution of 15.631 g (73.29 mmole) 1-(t-butoxycarbonyl)-4-formylpiperidine (from Step B2 above) in 100 mL methylene chloride was added to the resulting brown suspension with stirring and cooling over 40 minutes. After one hour, 200 mL ether and 400 mL hexanes was added. The top suspension was filtered through Celite, and the residue was resuspended in 150 mL methylene chloride and treated with 300 mL ether. The mixture was filtered, and the solid was washed with hexanes until the total filtrate was 2 L. The filtrate was filtered again through Celite and washed with hexanes. The filtrate was washed with 100 mL 5% sodium bicarbonate, 300 mL water (2×), and 150 mL brine. The organic layer was dried over sodium sulfate and concentrated under vacuum to give 53.5 g crude product as a yellowish solid. Flash chromatography (FC) on 250 g silica gel (0˜15% ethyl acetate in hexanes) gave 21.595 g title compound as a white solid.

1. temperaturecooling over 1.75 h
2. temperaturecooling over 40 minutes
3. waitAfter one hour
4. filtrationThe top suspension was filtered through Celite
5. additiontreated with 300 mL ether
6. filtrationThe mixture was filtered
7. washthe solid was washed with hexanes until the total filtrate
8. filtrationThe filtrate was filtered again through Celite
9. washwashed with hexanes
10. washThe filtrate was washed with 100 mL 5% sodium bicarbonate, 300 mL water (2×), and 150 mL brine
11. dry with materialThe organic layer was dried over sodium sulfate
12. concentrationconcentrated under vacuum
13. customto give 53.5 g crude product as a yellowish solid