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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692049Generated: October 29, 2026

Water → 4-Chloro-3-difluoromethyl-N-methylpyrazole

https://huagongshe.com/reaction/1692049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
Reactant3-(Difluoromethyl)-1-methyl-1H-pyrazoleHCID 54241061—
Reactant5-(difluoromethyl)-1-methyl-1H-pyrazoleHCID 66901778—
SolventDimethylformamideHCID 6228—
Product4-Chloro-3-difluoromethyl-N-methylpyrazoleHCID 6690174888%

Reaction Conditions

Temperature60 °C

Reaction Steps

At 0-5° C., a solution of N-chlorosuccinimide (NCS, 12.6 g, 0.09 mol) in dimethyl-formamide (DMF, 70 ml) was added dropwise to a solution of 3-difluoromethyl-N-methylpyrazole (14.9 g, 0.09 mol, 83.7% pure according to GC analysis) comprising, as minor component, 4.1% of 5-difluoromethyl-N-methylpyrazole, based on the total amount of the isomer mixture, in DMF (30 ml). The reaction mixture was then heated at 60° C. and stirred for a further 12 h. With stirring, the reaction mixture was then poured into water (1000 ml) and extracted twice with methyl tert-butyl ether (MTBE, 150 ml). The organic phases were combined, washed with a saturated aqueous solution of NaCl, dried over magnesium sulfate, filtered and then freed from the solvent under reduced pressure. 4-Chloro-3-difluoromethyl-N-methylpyrazole was obtained as an oil (17.6 g; purity: 78.4% according to GC analysis) comprising 3.7% of unreacted 5-difluoromethyl-N-methylpyrazole. This corresponds to a yield of 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153820B2
Source datasetuspto-grants-2012_04
ORD IDord-717c12a859ae47b2912ea90d6bec6775
Source noteuspto-grants-2012_04