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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377667Generated: October 30, 2026

Water → 3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-phenylmethylamino-4-trifluoroacetylpyrazole

https://huagongshe.com/reaction/377667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoroacetylpyrazoleHCID 18699459—
SolventDimethylformamideHCID 6228—
Product3-Cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-phenylmethylamino-4-trifluoroacetylpyrazoleHCID 19356477—

Reaction Steps

To a stirred solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoroacetylpyrazole (1 g) in anhydrous N,N-dimethylformamide (4 ml) at room temperature was added potassium carbonate (0.7 g), then benzyl bromide (228 μl). The mixture was stirred at room temperature for 40 minutes. Water (50 ml) was then added, and the mixture was extracted with ether (50 ml, ×2). The combined organic layers were washed with water (50 ml), dried (Na2SO4), filtered and evaporated. The residue was purified by column chromatography on silica gel (50 g) eluted with dichloromethane. Combination and evaporation of suitable fractions gave the title compound as a white solid, m.p 75-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028096
Source datasetuspto-grants-2000_02
ORD IDord-5b65e920b7d9445ab30facbd513c3ba9
Source noteuspto-grants-2000_02