Methylhydrazine → 5-Fluoro-1-methyl-3-pentafluoroethyl-4-trifluoromethyl-1H-pyrazole

HRID 623391

반응식

HRID 623391 반응식
C(Cl)Cl.[F:4][C:5](F)(F)[C:6]([C:16]([F:19])([F:18])[F:17])=[C:7](F)[C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10].CCN(CC)CC.[CH3:29][NH:30][NH2:31]>O>[CH3:29][N:30]1[C:5]([F:4])=[C:6]([C:16]([F:19])([F:18])[F:17])[C:7]([C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10])=[N:31]1

참가 물질

6

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온도
0 °C

실험 절차

In a 3-kneck flask equipped with condenser, thermometer, and a dropping funnel 130 ml methylene chloride and perfluoro-2-methyl-2-pentene (19.6 g, 0.065 mol) was placed and then 15 ml water were added. The mixture was cooled to 0° C. and Et3N (16.4 g, 0.16 mol) was added at a temperature ranging from 0° C. to 5° C. The mixture was stirred at this temperature for 15 min and 40% solution of methylhydrazine in water (7.4 g) was slowly added to this mixture at 0° C. The reaction mixture was stirred for 1 h at 5° C. and finally for 1.5 h at 20° C. The mixture was washed with water (3×50 ml), the organic layer was dried over Na2SO4 and the solvent was distilled off under atmospheric pressure. The crude product was purified via vacuum distillation. The yield of N-methyl-3-pentafluoroethyl-4-trifluoromethyl-5-fluoro-1H-pyrazole was 13.9 g. (75%), boiling point 62-65° C. at 17 mbar.

후처리

  1. customIn a 3-kneck flask equipped with condenser
  2. customranging from 0° C. to 5° C
  3. stirringThe reaction mixture was stirred for 1 h at 5° C. and finally for 1.5 h at 20° C
  4. washThe mixture was washed with water (3×50 ml)
  5. dry with materialthe organic layer was dried over Na2SO4
  6. distillationthe solvent was distilled off under atmospheric pressure
  7. distillationThe crude product was purified via vacuum distillation

출처 및 근거

ORD 기록
ord-067a6423e6c84c1fa595024d37d71e63
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09302994B2

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