反应 #2122481
ord-12db9e4a17a34c36982881ee8abcb862
反应方程式
(2,5-dimethyl-phenyl)-acetyl chloride
4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester
4-dimethylaminopyridine DMAP
→
4-[2-(2,5-dimethyl-phenyl)-acetoxy]-1-methoxy-piperidine-4-carboxylic acid ethyl ester
反应物
试剂
无
溶剂
反应条件
温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度The reaction mixture was warmed up to room temperature
- 2workup.WAITleft
- 3浓缩Then the reaction mixture was concentrated
- 4其他the crude product was purified by column chromatography on silica gel (ethyl acetate/cyclohexane first 1:15
实验过程
To a solution of 4-hydroxy-1-methoxy-piperidine-4-carboxylic acid ethyl ester (1.0 g, 4.92 mmol) in 10 ml pyridine under argon was added 4-dimethylaminopyridine DMAP (30 mg, 0.25 mmol). The solution was cooled down to 0° C., then (2,5-dimethyl-phenyl)-acetyl chloride (0.99 g, 5.4 mmol) was added dropwise. The reaction mixture was warmed up to room temperature and left stirring for 5 days. Then the reaction mixture was concentrated and the crude product was purified by column chromatography on silica gel (ethyl acetate/cyclohexane first 1:15, then 1:9) to give pure 4-[2-(2,5-dimethyl-phenyl)-acetoxy]-1-methoxy-piperidine-4-carboxylic acid ethyl ester (compound P3.2) as light yellow oil. Yield: 530 mg.