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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692048Generated: November 1, 2026

Water → 4-Bromo-3-(difluoromethyl)-1-methyl-1H-pyrazole

https://huagongshe.com/reaction/1692048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(Difluoromethyl)-1-methyl-1H-pyrazoleHCID 54241061—
Reactant5-(difluoromethyl)-1-methyl-1H-pyrazoleHCID 66901778—
SolventDimethylformamideHCID 6228—
Product4-Bromo-3-(difluoromethyl)-1-methyl-1H-pyrazoleHCID 4424926489%

Reaction Steps

At from 3 to 5° C., a solution of N-bromosuccinimide (NBS, 54 g, 0.3 mol) in dimethyl-formamide (DMF, 100 ml) was added dropwise to a solution of 3-difluoromethyl-N-methylpyrazole (49.3 g, 0.3 mol; 81.4% pure according to GC analysis) comprising, as minor component, 5.2% of 5-difluoromethyl-N-methylpyrazole, based on the total amount of the isomer mixture, in DMF (100 ml). The reaction mixture was then warmed to room temperature 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, 300 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-Bromo-3-difluoromethyl-N-methylpyrazole was obtained as an oil (76.6 g; purity: 74.2% according to GC analysis) comprising 4.5% of unreacted 5-difluoromethyl-N-methylpyrazole. This corresponds to a yield of 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153820B2
Source datasetuspto-grants-2012_04
ORD IDord-d2e77615b8c247d3a67974c3b5fbc65d
Source noteuspto-grants-2012_04