反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a suspension of 5-acetyl-8-(benzyloxy)quinolin-2(1H)-one (19.4 g, 66.4 mmol) in anhydrous THF (240 mL) and anhydrous methanol (165 mL) was added a solution of tetra-n-butylammonium tribromide (54.5 g, 113.0 mmol) in anhydrous THF (130 mL) dropwise over 1.5 hours. The resulting solution was stirred at RT overnight before concentrating under reduced pressure without heating. The residue was re-dissolved in methanol (200 mL). Saturated aqueous ammonium chloride solution (390 mL) was added with ice-cooling. The resulting suspension was filtered, and the solid washed with water and air-dried under vacuum. The solid was suspended in DCM and methanol (1:1 v/v, 100 mL) for 90 minutes. The solid was collected by filtration, washed with DCM and air-dried to afford the title compound (18.0 g, 73%).
WORKUP
后处理
- concentrationbefore concentrating under reduced pressure
- temperaturewithout heating
- dissolutionThe residue was re-dissolved in methanol (200 mL)
- additionSaturated aqueous ammonium chloride solution (390 mL) was added with ice-
- temperaturecooling
- filtrationThe resulting suspension was filtered
- washthe solid washed with water
- customair-dried under vacuum
- waitmethanol (1:1 v/v, 100 mL) for 90 minutes
- filtrationThe solid was collected by filtration
- washwashed with DCM
- customair-dried