反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 2.5 °C
PROCEDURE
实验过程
Ethylene oxide (40 mL) was added to a mixture of the ester of Example 35j (1 g, 2.72 mmol), acetic acid (15 mL) and water (15 mL) at 0-5° C. THF (2 mL) was added and the reaction mixture was stirred at 0-5° C. for 4 h and then left for overnight at room temperature. It was treated with water and aqueous Na2CO3 solution to neutral pH followed by extraction with ethyl acetate. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography (silica gel) to obtain the title compound. Yield: 0.9 g, (73%); 1H NMR (DMSO-d6): δ 2.8 (s, 3H, CH3), 3.6 (t, 4H, 2CH2), 3.7, (t, 4H, 2CH2), 3.9, (s, 3H, OCH3), 5.2, (s, 2H, CH2) 6.9, (s, 2H, Ar), 8.2 (s, 2H, Ar); MS: m/e (CI+) 455 (M+1).
WORKUP
后处理
- waitleft for overnight at room temperature
- extractionfollowed by extraction with ethyl acetate
- washThe organic layer was washed with water, brine
- customdried
- concentrationconcentrated
- custompurified