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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854127Generated: October 26, 2026

Water → 4-(Chloromethyl)-5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1H-pyrazole

https://huagongshe.com/reaction/854127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSulfuryl chlorideHCID 24648—
Reactant5-(Difluoromethoxy)-1,4-dimethyl-3-(trifluoromethyl)-1H-pyrazoleHCID 23075667—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Chloromethyl)-5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1H-pyrazoleHCID 2307568336.3%

Reaction Steps

To a solution of 11.5 g (50.0 mmol) of 5-difluoromethoxy-1,4-dimethyl-3-trifluoromethyl-1H-pyrazole in 50 ml of carbon tetrachloride were added 10.1 g (75.0 mmol) of sulfuryl chloride and 0.8 (5.0 mmol) of α,α′-azobisisobutyronitrile, followed by heating and refluxing under stirring. The reaction solution was externally irradiated with a light for 11 hours. After the completion of the reaction was confirmed, the reaction solution was poured into water and extracted with chloroform. The resulting organic layer was washed with water and saline, successively, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the residue was purified by silica gel column chromatography to obtain 4.8 g (purity: 83.4%, yield: 30.3%) of 4-chloromethyl-5-difluoromethoxy-1-methyl-3-trifluoromethyl-1H-pyrazole as a colorless transparent liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256298B2
Source datasetuspto-grants-2007_08
ORD IDord-d46e9b43e8914b54a90475f172aed385
Source noteuspto-grants-2007_08