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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274352Generated: November 1, 2026

Water → 5-Amino-4-(2-chlorofuran-3-yl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole

https://huagongshe.com/reaction/1274352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantChlorosuccinimideHCID 31398—
Reactant5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(3-furanyl)pyrazoleHCID 22120906—
SolventAcetonitrileHCID 6342—
Product5-Amino-4-(2-chlorofuran-3-yl)-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoleHCID 22120915—

Reaction Steps

To a solution of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-(furan-3-yl)pyrazole (0.095 g) in acetonitrile (6 ml) was added N-chlorosuccinimide (0.0345 g). The mixture was left at room temperature for 1.5 hours and then poured into ether (50 ml) and water (50 ml). The layers were separated and the aqueous phase extracted with a second portion of ether (50 ml). The combined organic layers were washed with water (25 ml), then dried (Na2SO4) and evaporated. The residue was purified by column chromatography on silica gel (10 g) eluted with dichloromethane. Combination and evaporation of suitable fractions gave the title compound as a white solid, m.p. 153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156782
Source datasetuspto-grants-2000_12
ORD IDord-bc9c5a0b9c534afd98ed8efa142c5d6a
Source noteuspto-grants-2000_12