反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 25 °C
PROCEDURE
实验过程
A solution of (3-chloro-4-methylsulfanyl-phenyl)-acetic acid (7.00 g, 32.30 mmol) in methanol (150 mL) was treated slowly with concentrated sulfuric acid (2.8 mL, 52.65 mmol). The resulting reaction mixture was heated under reflux for 1.5 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to remove methanol. The residue was diluted with ethyl acetate (500 mL). The organic phase was successively washed with a saturated aqueous sodium bicarbonate solution (1×200 mL) and a saturated aqueous sodium chloride solution (1×200 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to afford (3-chloro-4-methylsulfanyl-phenyl)-acetic acid methyl ester (7.41 g, 99.4%) as a light yellow oil: EI-HRMS m/e calcd for C10H11ClO2S (M+) 230.0168. found 230.0166.
WORKUP
后处理
- customThe resulting reaction mixture
- temperaturewas heated
- temperatureunder reflux for 1.5 h
- concentrationconcentrated in vacuo
- customto remove methanol
- additionThe residue was diluted with ethyl acetate (500 mL)
- washThe organic phase was successively washed with a saturated aqueous sodium bicarbonate solution (1×200 mL)
- dry with materiala saturated aqueous sodium chloride solution (1×200 mL), dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo