反应 #67952
ord-c846f63164644d04a5a0217a7ae5a053
反应方程式
反应物
试剂
反应条件
后处理
- 1workup.ADDITIONwere added
- 2workup.STIRRINGstirred at the same temperature for 30 minutes
- 3workup.STIRRINGstirred at the same temperature for 30 minutes
- 4workup.STIRRINGthe reaction mixture was stirred for 1 hour
- 5温度under reflux
- 6温度by heating
- 7其他The organic layer was separated
- 8萃取the aqueous layer was extracted with chloroform
- 9洗涤the resultant solution was washed with an aqueous saturated sodium chloride solution
- 10干燥dried over anhydrous magnesium sulfate
- 11其他the solvent was removed under reduced pressure
实验过程
To 5 mL of a dichloromethane solution containing 0.50 g of tert-butyl 4-amino-4-methylpiperidine-1-carboxylate, 0.38 g of 2,3-dihydro-1,4-benzodioxin-6-carbaldehyde and 0.13 mL of acetic acid were added, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes, and then the reaction mixture was stirred for 1 hour under reflux by heating. Thereto were added chloroform and an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, and the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.81 g of a light brown oily substance, tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate.