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
- 0 °C
PROCEDURE
实验过程
4-Butyrolactone (11.93 mL, 0.155 mol) was dissolved in anhydrous THF and cooled to 0° C. Phenylmagnesium bromide (3M in ether, 112 mL) was added dropwise over 30 minutes to the reaction under N2. After the addition, the reaction was warmed to room temperature overnight. Additional phenylmagnesium bromide (3M in ether, 103 mL) was added, and the reaction stirred at room temperature overnight. The reaction was quenched with saturated NH4Cl (150 mL). Ether (200 mL) and 10% HCl (100 mL) were added. The organic layer was separated and washed with 10% HCl (100 mL), brine (100 mL), and then dried over MgSO4. The solution was filtered, concentrated, and the crude material chromatographed on silica gel eluting with 50% EtOAc/Hexanes to give 26.94 g (72%) of desired product as an off-white solid.
WORKUP
后处理
- additionAfter the addition
- temperaturethe reaction was warmed to room temperature overnight
- customThe reaction was quenched with saturated NH4Cl (150 mL)
- additionEther (200 mL) and 10% HCl (100 mL) were added
- customThe organic layer was separated
- washwashed with 10% HCl (100 mL), brine (100 mL)
- dry with materialdried over MgSO4
- filtrationThe solution was filtered
- concentrationconcentrated
- customthe crude material chromatographed on silica gel eluting with 50% EtOAc/Hexanes