反応 #586135

ord-2c5671f66d5d46b186019dbd66010b51

反応方程式

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
収率 18.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The resulting reaction mixture
  2. 2
    抽出the organic matters were extracted with 20 ml of ethyl acetate twice
  3. 3
    洗浄washed with 30 ml of water twice
  4. 4
    乾燥dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
  6. 6
    その他Purification of the residue by thin layer chromatography

実験手順

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.).

出典

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