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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623391Generated: October 26, 2026

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

https://huagongshe.com/reaction/623391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantPerfluoro(2-methyl-2-pentene)HCID 74105—
SolventWaterHCID 962—
Product5-Fluoro-1-methyl-3-pentafluoroethyl-4-trifluoromethyl-1H-pyrazoleHCID 13510273—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302994B2
Source datasetuspto-grants-2016_04
ORD IDord-067a6423e6c84c1fa595024d37d71e63
Source noteuspto-grants-2016_04