反应 #586135

ord-2c5671f66d5d46b186019dbd66010b51

反应方程式

O
water
COC(=O)c1ccc(-c2c[nH]nc2C(F)(F)F)cc1Cl
methyl 2-chloro-4-(3-trifluoromethylpyrazolyl)benzoate
CCCS
1-propanethiol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCSc1cc(-c2c[nH]nc2C(F)(F)F)ccc1C(=O)OC
methyl 2-propylthio-4-(3-trifluoromethylpyrazolyl)benzoate
收率 18.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The resulting reaction mixture
  2. 2
    萃取the organic matters were extracted with 20 ml of ethyl acetate twice
  3. 3
    洗涤washed with 30 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
  6. 6
    其他Purification of the residue by thin layer chromatography

实验过程

1.52 g (5.0 mmol) of methyl 2-chloro-4-(3-trifluoromethylpyrazolyl)benzoate, 0.66 g (8.6 mmol) of 1-propanethiol and 0.83 g (6.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at 60° C. for 24 hours. The resulting reaction mixture was poured into 50 ml of water, and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, washed with 30 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by thin layer chromatography afforded 0.31 g of methyl 2-propylthio-4-(3-trifluoromethylpyrazolyl)benzoate as a white powder (m.p. 114-116° C.).

来源

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