反应 #169669
ord-d9dbf7df017e4037b9fd736da651c8e5
反应方程式
niacin
2-Hydroxy-succinic acid 4-(4-allyl-2-methoxy-phenyl)ester
N-ethyldiisopropyl amine
EDCI.HCl
HOBt
→
oil
收率 58.4%
2-(Pyridine-3-carbonyloxy)-succinic acid 4-(4-allyl-2-methoxy-phenyl)ester 1-methyl ester
收率 58.4%
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1workup.STIRRINGthe reaction mixture was stirred at room temperature (25° C.) over a period of 5 h
- 2洗涤washed with water (4×50 mL)
- 3干燥dried over sodium sulphate
- 4其他The crude product obtained upon evaporation of volatiles
- 5其他was purified by column chromatography
实验过程
To a suspension of niacin (90 mg, 0.7 mmol) in dichloromethane (10.0 mL) were added N-ethyldiisopropyl amine (0.58 mL, 3.0 mmol), EDCI.HCl (380 mg, 2.0 mmol), HOBt (50 mg, 0.3 mmol) at 0° C. and stirred for 15 min. Then 2-Hydroxy-succinic acid 4-(4-allyl-2-methoxy-phenyl)ester (200 mg, 0.6 mmol) was added at the same temperature and the reaction mixture was stirred at room temperature (25° C.) over a period of 5 h. The reaction mixture was diluted with DCM (150 mL), washed with water (4×50 mL) and dried over sodium sulphate. The crude product obtained upon evaporation of volatiles was purified by column chromatography to obtain pale yellow viscous oil (140 mg, 51%).