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
CONDITIONS
反应条件
- 温度
- -78 °C
PROCEDURE
实验过程
To a solution of (-)-calanolide A (341 mg, 0.922 mmol) in anhydrous methylene chloride (5 mL) at -78° C. under N2 was added a solution of diethylamidosulfur trifluoride (DAST, 178 mg, 1.11 mmol) in methylene chloride (1 mL) and the resulting yellow solution stirred at -78° C. for 4 hours. The reaction was quenched with 0.5 mL methanol, then allowed to warm to room temperature. The solution was diluted with methylene chloride (20 mL), then washed with water (50 mL) and saturated brine (50 mL). After drying over magnesium sulfate, the solution was filtered and evaporated to provide a light yellow solid. TLC analysis (silica gel, 3% methanol in methylene chloride) showed two components, one fast-moving and one slow. The material was chromatographed through 80 g silica gel, eluting with 1% methanol in CH2Cl2, and the fractions containing the respective components combined and evaporated to afford 198 mg (61% yield) of compound 22 and 75.3 mg (22%) of (-)-calanolide B.
WORKUP
后处理
- customThe reaction was quenched with 0.5 mL methanol
- temperatureto warm to room temperature
- additionThe solution was diluted with methylene chloride (20 mL)
- washwashed with water (50 mL) and saturated brine (50 mL)
- dry with materialAfter drying over magnesium sulfate
- filtrationthe solution was filtered
- customevaporated
- customto provide a light yellow solid
- customThe material was chromatographed through 80 g silica gel
- washeluting with 1% methanol in CH2Cl2
- additionthe fractions containing the respective components
- customevaporated