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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352415Generated: October 31, 2026

Hydrogen Bromide → 4-Bromo-1-(2,4,6-trichlorophenyl)-3-(trifluoromethyl)-1H-pyrazole

https://huagongshe.com/reaction/2352415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant(2,4,6-Trichlorophenyl)hydrazineHCID 79234—
Reactant3-Buten-2-one, 3-bromo-4-ethoxy-1,1,1-trifluoro-HCID 3729078—
SolventEthanolHCID 702—
Product4-Bromo-1-(2,4,6-trichlorophenyl)-3-(trifluoromethyl)-1H-pyrazoleHCID 1427419330.4%

Reaction Steps

2.3 g (0.01 mole) of 3-bromo-4-ethoxy-1,1,1-trifluorobut-3-en-2-one are added to a solution of 4.2 g (0.02 mol) of 2,4,6-trichlorophenyl-hydrazine in 100 ml of ethanol which contains 0.01 mole hydrogen bromide. The mixture is refluxed for 5 hours and then concentrated under reduced pressure, and ice water is added to the residue. Extraction with dichloromethane, washing with saturated sodium chloride solution until neutral, clarification over anhydrous sodium sulphate and concentration gives 4.6 g of a crude product, which is chromatographed on 120 g of silica gel using toluene/petroleum ether (ratio 1:1). 1.2 g of 4-bromo-1-(2,4,6-trichloro-phenyl)-3-trifluoromethylpyrazole of melting point 93°-94° C. (from petroleum ether) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876393
Source datasetuspto-grants-1989_10
ORD IDord-e323f4fb137046658e9e11a4e3f5af54
Source noteuspto-grants-1989_10