Реакция #586147
ord-51a1ae9b48084baeacafa6322f9e41f9
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Промывкаwashed with 30 ml of ethyl acetate
- 2Экстракцияextracted with 50 ml of ethyl acetate twice
- 3Промывкаwashed with 50 ml of water twice
- 4Сушкаdried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONThe ethyl acetate was distilled off under reduced pressure
Методика
5.0 g (18.4 mmol) of 2-chloro-4-(3-trifluoromethylpyrazolyl)benzonitrile in N,N-dimethylformamide was stirred together with 1.86 g (23.9 mmol) of sodium sulfide at 120° C. for 30 minutes. The reaction mixture was cooled to room temperature, mixed with 100 ml of water, washed with 30 ml of ethyl acetate, and the aqueous layer was adjusted at pH 5-6 with citric acid, and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layers were combined, washed with 50 ml of water twice and dried over anhydrous magnesium sulfate. The ethyl acetate was distilled off under reduced pressure to obtain 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 97.6%) as a pale yellow powder, which was used in Example 1 (2) as the starting material.