Tert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate → 3-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole

HRID 499993ノート

反応式

HRID 499993 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([F:12])[C:3]=1[O:13][C:14]1[CH:18]=[C:17]([CH3:19])[N:16](C(OC(C)(C)C)=O)[N:15]=1>C(OCC)(=O)C>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:9])[F:10])[CH:5]=[C:4]([F:12])[C:3]=1[O:13][C:14]1[CH:18]=[C:17]([CH3:19])[NH:16][N:15]=1

参加物

3

反応物 1

HCID 57548571Tert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate

生成物 1

HCID 178624283-(2-Chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole収率 89%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

To an ethyl acetate (100 mL) solution of tert-butyl 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole-1-carboxylate (49.7 g, 126 mmol) was added 3 mol/L of HCL (40 mL), and the mixture was refluxed under heating for 2 hours. After completion of the reaction, the reaction mixture was consecutively washed with water and a 1 mol/L sodium hydroxide aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off to give a white solid of 3-(2-chloro-6-fluoro-4-trifluoromethylphenyloxy)-5-methylpyrazole (33.0 g, yield: 89.0%). Melting point: 116˜117° C., 1H-NMR (CDCl3, TMS, ppm): δ2.24 (s, 3H), 5.69 (s, 1H), 7.36 (dd, J=1.8 Hz, JHF=9.4 Hz, 1H), 7.50-7.60 (m, 1H), 9.00-9.30 (brs, 1H).

後処理

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 2 hours
  3. customAfter completion of the reaction
  4. washthe reaction mixture was consecutively washed with water
  5. dry with materiala 1 mol/L sodium hydroxide aqueous solution and dried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off

出典と根拠

ORDレコード
ord-342196a38a7e457c9688c647f4c23adb
出典データセット
uspto-grants-2010_08
特許番号
US07767827B2

反応ノート

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