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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623392Generated: October 26, 2026

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

https://huagongshe.com/reaction/623392

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 1351027385%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 21 3-kneck flask equipped with condenser, thermometer, and a dropping funnel 1300 ml methylene chloride and perfluoro-2-methyl-2-pentene (197 g, 0.65 mol) was placed, and then 117 ml water were added. The mixture was cooled to −0° C. and Et3N (164 g, 1.62 mol) was added at a temperature ranging from −5° to 5° C. The mixture was stirred at this temperature for 15 min and a solution of 75 ml N-methylhydrazine in water (40% w.w.) was slowly added to this mixture at 5° C. within 2 h. The reaction mixture was stirred for 15-20 h at 20° C. The mixture was washed with water, 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 158 g (85% yield). Boiling point 62-67° C. at 15-20 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302994B2
Source datasetuspto-grants-2016_04
ORD IDord-5dcbc15387f34b1694196be3322e1feb
Source noteuspto-grants-2016_04