HRID2282955
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
- -15 °C
PROCEDURE
实验过程
A mixture of (tert-butoxy)-N-[1-(3-ethoxy-4methoxyphenyl)-3-oxobutyl]carboxamide (2.0 g, 5.92 mmol) and sodium borohydride (0.4 g, 12.0 mmol) in methanol (40 mL) and tetrahydrofuran (10 mL) was stirred at −10 to −20° C. for 4 hours. The mixture was quenched with water (10 mL) and then concentrated in vacuo to afford an oil. The oil was dissolved in ethyl acetate and washed with water, brine, dried, and concentrated in vacuo to afford an oil. The oil was purified by chromatography (silica gel, methylene chloride:ethyl acetate 8:2) to give the two diasteromers of (tert-butoxy-N-[1-(3-ethoxy-4-methoxyphenyl)-3-hydroxybutyl)carboxamide:
WORKUP
后处理
- customThe mixture was quenched with water (10 mL)
- concentrationconcentrated in vacuo
- customto afford an oil
- washwashed with water, brine
- customdried
- concentrationconcentrated in vacuo
- customto afford an oil
- customThe oil was purified by chromatography (silica gel, methylene chloride:ethyl acetate 8:2)