反应详情

温度

-78 °C

A solution of (2-bromo-5-chlorophenyl)methanol (1.48 g, 6.68 mmol) in anhydrous THF (30 mL) was cooled to −78° C. and treated with the dropwise addition of n-BuLi (1.6 M in hexanes) (8.77 mL, 14.03 mmol), and the mixture was stirred for 30 minutes at −78° C., during which a thick white precipitate was observed. The dianion was treated with the dropwise addition of a solution of tert-butyl 4-oxopiperidine-1-carboxylate (1.465 g, 7.35 mmol) in THF (10 mL), and the mixture was stirred for 1 hour at −78° C., during which a yellow homogeneous solution was observed, then allowed to warm to room temperature and stirred overnight. The reaction was quenched with saturated ammonium chloride and the mixture was extracted 3× with ethyl acetate. The combined organic phases were washed with water and brine, then dried over sodium sulfate and concentrated in-vacuo. The residue was split into two equal fractions, and each was purified over a 40 g silica gel column via ISCO, eluting with a 10-100% EtOAc/Hexanes gradient over 15 minutes. The fractions from each run which contained the desired product were combined to yield the title compound (1.4 g, 4.10 mmol, 61.3% yield) as a colorless foam. MS (ESI+)=268, (M+H-tBuOH)+.

1. stirringthe mixture was stirred for 1 hour at −78° C., during which a yellow homogeneous solution
2. temperatureto warm to room temperature
3. stirringstirred overnight
4. customThe reaction was quenched with saturated ammonium chloride
5. extractionthe mixture was extracted 3× with ethyl acetate
6. washThe combined organic phases were washed with water and brine
7. dry with materialdried over sodium sulfate
8. concentrationconcentrated in-vacuo
9. customThe residue was split into two equal fractions
10. customeach was purified over a 40 g silica gel column via ISCO
11. washeluting with a 10-100% EtOAc/Hexanes
12. waitgradient over 15 minutes