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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078452Generated: October 31, 2026

Bromoform → HCID 10275860, compound

https://huagongshe.com/reaction/1078452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-Amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-3-(trifluoromethyl)-1H-pyrazole-4-carbonitrileHCID 10134900—
ProductHCID 10275860HCID 10275860—

Reaction Conditions

Temperature50 °C

Reaction Steps

A stirred mixture of 5-amino-4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole (3.89 g) and bromoform (13 ml) was treated with tert-butyl nitrite (2.26 ml) at room temperature. After 15 minutes the mixture was heated to 50° C. for 1 hour, and evaporated in vacuo to yield a red oil. This was purified by chromatography on silica (Merck, 40-230 mesh, 0.7 kg cm-2) eluting with a mixture of dichloromethane and petroleum ether (1:2) to furnish 5-bromo-4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole as a fawn solid m.p. 85°-87° C. (3.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547974
Source datasetuspto-grants-1996_08
ORD IDord-d8c0e650b97c43819249f2d6123c1a33
Source noteuspto-grants-1996_08