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 solution of (R)-7-(4-fluorophenyl)-7-(3-formyl-6-hydroxy-2,4,5-trimethylphenyl)heptanoic acid (0.43 g, 1.1 mmol) in tetrahydrofuran (7 ml) was added, under ice-cooling, sodium borohydride (21.0 mg). The mixture was stirred for two hours at room temperature, to which was added acetone, then the solvent was distilled off under reduced pressure. The residue was neutralized with 1N HCl, which was subjected to extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous saline solution, followed by drying over magnesium sulfate. The solvent was distilled off under reduced pressure to leave 0.38 g of (R)-7-(4-fluorophenyl)-7-(2-hydroxy-5-hydroxylmethyl-3,4,6-trimethylphenyl)heptanoic acid, whose spectral data are shown in [Table 4].
WORKUP
后处理
- temperaturecooling
- distillationthe solvent was distilled off under reduced pressure
- extractionwas subjected to extraction with ethyl acetate
- washThe organic layer was washed with water
- dry with materialby drying over magnesium sulfate
- distillationThe solvent was distilled off under reduced pressure