反应 #61856

反应方程式

3-methyl-1-(4′-fluoronaphth-1-yl)butan-1-one

phenyltrimethylammonium tribromide

→

2-bromo-1-(4′-fluoronaphth-1-yl)-3-methylbutan-1-one

溶剂

tetrahydrofuran

反应条件

后处理

1. 1
   其他then partitioned between petroleum ether and water
2. 2
   其他The organic layer was separated
3. 3
   洗涤washed with water, brine
4. 4
   干燥dried with sodium sulphate
5. 5
   过滤filtered
6. 6
   其他evaporated in vacuo

实验过程

To a solution of 3-methyl-1-(4′-fluoronaphth-1-yl)butan-1-one (7 g) in anhydrous tetrahydrofuran (80 ml) was added phenyltrimethylammonium tribromide (11.5 g). The resulting mixture was stirred overnight at ambient temperature then partitioned between petroleum ether and water. The organic layer was separated, washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo to yield crude 2-bromo-1-(4′-fluoronaphth-1-yl)-3-methylbutan-1-one. Sodium acetate (2.75 g) and anhydrous dimethylformamide (30 ml) were added and the resulting mixture was stirred at 80° C. for 5 hours. After cooling, the mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted once with ethyl acetate. The combined organic layers were washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo. The title compound (4.8 g) was obtained following silica gel column chromatography of the residue in 30-100% dichloromethane in petroleum ether.

来源