反応 #8185

反応方程式

3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole

ethanol

→

2-methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine

溶媒

tetrahydrofuran

反応条件

後処理

1. 1
   温度the mixture is cooled to ambient temperature
2. 2
   温度is warmed to 50° C
3. 3
   その他The catalyst is removed by filtration
4. 4
   洗浄the cake is rinsed with 50° C. tetrahydrofuran (4×50 mL)
5. 5
   濃縮The filtrate is concentrated to a solid which
6. 6
   その他is dried in a 50° C. vacuum oven

実験手順

A mixture of 3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole (25.0 g, 77.1 mmol), Raney Nickel® (9.5 g wet lump), and 3A ethanol (250 mL) is pressurized to 50 psig with H2 and is heated to 60° C. After 1 hour, the mixture is cooled to ambient temperature. The mixture is diluted with tetrahydrofuran (100 mL) and is warmed to 50° C. The catalyst is removed by filtration and the cake is rinsed with 50° C. tetrahydrofuran (4×50 mL). The filtrate is concentrated to a solid which is dried in a 50° C. vacuum oven to provide 22.41 (99%) of 2-methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine. MS (ES+) m/z 295 (100%).

出典