Reaction #710573

ord-067a6423e6c84c1fa595024d37d71e63

Reaction equation

CNN
methylhydrazine
ClCCl
methylene chloride
FC(=C(C(F)(F)F)C(F)(F)F)C(F)(F)C(F)(F)F
perfluoro-2-methyl-2-pentene
CCN(CC)CC
Et3N
Cn1nc(C(F)(F)C(F)(F)F)c(C(F)(F)F)c1F
N-Methyl-3-Pentafluoroethyl-4-Trifluoromethyl-5-Fluoro-1H-Pyrazole

Solvents

Conditions

Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherIn a 3-kneck flask equipped with condenser
  2. 2
    Otherranging from 0° C. to 5° C
  3. 3
    workup.STIRRINGThe reaction mixture was stirred for 1 h at 5° C. and finally for 1.5 h at 20° C
  4. 4
    WashThe mixture was washed with water (3×50 ml)
  5. 5
    Dryingthe organic layer was dried over Na2SO4
  6. 6
    workup.DISTILLATIONthe solvent was distilled off under atmospheric pressure
  7. 7
    workup.DISTILLATIONThe crude product was purified via vacuum distillation

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09302994B2uspto-grants-2016_04