反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Chloroacetyl chloride (4.88 mL) was added dropwise to a vigorously stirred mixture at 0° C. of potassium carbonate (17.43 g) in water (78 mL) and tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate (10.4 g) in ethyl acetate (92 mL). After 30 minutes at 0° C. the mixture was extracted with ethyl acetate and the organic layer dried over sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residue was dissolved in THF (200 mL) and added dropwise over 3 hours to a stirred solution under nitrogen and heated at reflux of potassium tert-butoxide (1M in tert-butanol, 75 mL) and THF (250 mL). The mixture was cooled to room temperature and allowed to stir for 18 hours. Most of the solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and brine, the aqueous layer was re-extracted with ethyl acetate and the combined organics were dried over sodium sulfate, filtered and the solvent removed under reduced pressure. The residue was purified by trituration with a mixture of ether (30 mL) and isohexane (20 mL) to afford the subtitled product. Yield 8.20 g.
WORKUP
后处理
- extractionAfter 30 minutes at 0° C. the mixture was extracted with ethyl acetate
- dry with materialthe organic layer dried over sodium sulfate
- filtrationfiltered
- customthe solvent evaporated under reduced pressure
- dissolutionThe residue was dissolved in THF (200 mL)
- additionadded dropwise over 3 hours to a stirred solution under nitrogen
- temperatureheated
- temperatureat reflux of potassium tert-butoxide (1M in tert-butanol, 75 mL) and THF (250 mL)
- customMost of the solvent was removed under reduced pressure
- customthe residue partitioned between ethyl acetate and brine
- extractionthe aqueous layer was re-extracted with ethyl acetate
- dry with materialthe combined organics were dried over sodium sulfate
- filtrationfiltered
- customthe solvent removed under reduced pressure
- customThe residue was purified by trituration with a mixture of ether (30 mL) and isohexane (20 mL)