反应 #80269

反应方程式

phenylchloroformate

N,N-dimethylethanolamine

triethylamine

→

8

N-[2-((Phenoxycarbonyl)oxy)ethyl]-N,N-dimethylamine

溶剂

toluene

toluene

反应条件

后处理

1. 1
   其他To a 500 ml three-necked round-bottomed flask equipped with an internal thermometer
2. 2
   温度reflux
3. 3
   workup.ADDITIONcondenser, mechanical stirrer, addition funnel, and argon inlet
4. 4
   workup.ADDITIONAfter addition
5. 5
   温度the mixture is heated
6. 6
   温度to reflux for 3 h
7. 7
   洗涤The cooled mixture is washed with saturated sodium bicarbonate solution (2×100 ml) and water (100 ml)
8. 8
   干燥The organic phase is dried over MgSO4
9. 9
   过滤filtered
10. 10
    浓缩concentrated first by rotary evaporation at 50° C. (water aspirator vacuum)

实验过程

To a 500 ml three-necked round-bottomed flask equipped with an internal thermometer, reflux condenser, mechanical stirrer, addition funnel, and argon inlet are added N,N-dimethylethanolamine (25.00 g, 0.281 mol), toluene (200 ml), and triethylamine (31.21 g, 0.309 mol). The mixture is treated with a solution of phenylchloroformate (43.91 g, 0.281 mol) dissolved in 50 ml of toluene over 15 min. After addition is complete, the mixture is heated to reflux for 3 h. The cooled mixture is washed with saturated sodium bicarbonate solution (2×100 ml) and water (100 ml). The organic phase is dried over MgSO4, filtered, and concentrated first by rotary evaporation at 50° C. (water aspirator vacuum) and then at 60° C. (0.05 mmHg) in a Kugelrohr oven to give 8 as a light yellow oil, 49.93 g (85%) that crystallizes on standing.

来源