反应 #2171081
ord-fc6fbccb965540f7b6539c1546cf8e9a
反应方程式
反应条件
后处理
- 1其他Volatile material was removed by evaporation
- 2其他the residue was partitioned between saturated sodium bicarbonate (100 ml) and ethyl acetate (100 ml)
- 3其他The organic layer was separated
- 4洗涤washed with saturated sodium chloride (2×100 ml)
- 5其他dried
- 6浓缩Concentration
实验过程
4-(2,3-Epoxypropoxy)nitrobenzene (obtained as described in Synthetic Communications, 1994, 24, 833; 4.3 g) was dissolved in methanol (30 ml) and DMF (10 ml). A solution of dimethylamine in methanol (2M, 17 ml) was added and the mixture was stirred overnight. Volatile material was removed by evaporation and the residue was partitioned between saturated sodium bicarbonate (100 ml) and ethyl acetate (100 ml). The organic layer was separated and washed with saturated sodium chloride (2×100 ml) and dried. Concentration gave the product as an oil that slowly crystallised under high vacuum (4.79 g, 89.9%). NMR (CDCl3): 2.33 (s, 6H), 2.98 (m, 1H), 2.54 (m, 1H), 4.00 (m, 3 H), 7.00 (d, 2H), 8.20 (d, 2H); MS (MH+): 241.