反应 #586147

ord-51a1ae9b48084baeacafa6322f9e41f9

反应方程式

O
water
N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1Cl
2-chloro-4-(3-trifluoromethylpyrazolyl)benzonitrile
[Na+].[Na+].[S-2]
sodium sulfide
N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1S
2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile
收率 97.6%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤washed with 30 ml of ethyl acetate
  2. 2
    萃取extracted with 50 ml of ethyl acetate twice
  3. 3
    洗涤washed with 50 ml of water twice
  4. 4
    干燥dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONThe ethyl acetate was distilled off under reduced pressure

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767626B2uspto-grants-2010_08