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
A mixture of (3-dimethylcarbamoylsulfanyl-phenyl)-acetic acid methyl ester (2.0 g, 7.9 mmol), potassium hydroxide (1.4 g, 24 mmol) methanol (50 mL), and water (5 mL) is stirred at reflux 3 hr. The mixture is concentrated, and product partitioned between 1M aqueous hydrochloric acid (50 mL) and ethyl acetate (3×75 mL). The combined extracts are dried over anhydrous magnesium sulfate, filtered and concentrated. The residue is taken up in methanol (50 mL), 2 mL concentrated sulfuric acid is added, and the mixture refluxed 3 hr. The mixture is concentrated, and the residue purified by silica chromatography eluting with 7:3 hexanes:ethyl acetate to afford the title compound as a pale yellow oil, 1.0 g, 69%. MS M++1 183. The structure is confirmed by 1H NMR spectroscopy.
WORKUP
后处理
- temperatureat reflux 3 hr
- concentrationThe mixture is concentrated
- customproduct partitioned between 1M aqueous hydrochloric acid (50 mL) and ethyl acetate (3×75 mL)
- dry with materialThe combined extracts are dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- addition2 mL concentrated sulfuric acid is added
- temperaturethe mixture refluxed 3 hr
- concentrationThe mixture is concentrated
- customthe residue purified by silica chromatography
- washeluting with 7:3 hexanes