反应详情

温度

25 °C

A solution of 3-cyclopentyl-2-(4-methanesulfonyl-3-trifluoromethyl-phenyl)-propionic acid ethyl ester (707 mg, 1.80 mmol in tetrahydrofuran/water (24 mL, 3:1) was treated with lithium hydroxide (166 mg, 3.97 mmol). The reaction was stirred at 25° C. for 24 h. At this time, the reaction concentrated in vacuo. The residue was diluted with water (25 mL) and extracted with diethyl ether (1×15 mL). The aqueous layer was acidified to pH=1 with a 2N aqueous hydrochloric acid solution, and extracted with chloroform (3×25 mL). The combined organic layers were washed with water (1×25 mL) and a saturated aqueous sodium chloride solution (3×25 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 3-cyclopentyl-2-(4-methanesulfonyl-3-trifluoromethyl-phenyl)-propionic acid (426.7 mg, 65%) as a white solid: mp 122–123° C.; EI-HRMS m/e calcd for C16H19F3O4S (M+) 364.0956 found 364.0956.

1. concentrationAt this time, the reaction concentrated in vacuo
2. additionThe residue was diluted with water (25 mL)
3. extractionextracted with diethyl ether (1×15 mL)
4. extractionextracted with chloroform (3×25 mL)
5. washThe combined organic layers were washed with water (1×25 mL)
6. dry with materiala saturated aqueous sodium chloride solution (3×25 mL), dried over magnesium sulfate
7. filtrationfiltered
8. concentrationconcentrated in vacuo