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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842147Generated: October 30, 2026

Pyridine → 5-Acetamido-3-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole

https://huagongshe.com/reaction/842147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
Reactant5-Amino-3-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoleHCID 22618394—
SolventChloroformHCID 6212—
Product5-Acetamido-3-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoleHCID 2261845895.3%

Reaction Steps

Pyridine (4.0 ml) was added dropwise to a stirred solution of 5-amino-3-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole (5.0 g), acetyl chloride (3.0 g) and dry chloroform (30 ml), causing an exothermic reaction (maximum temperature 60° C.). The reaction mixture was stirred at laboratory temperature for 2 h and evaporated to dryness. The residue was dissolved in ethanol (25 ml), ammonia solution (d. 0.880; 25 ml) was added, and the solution was boiled under reflux for 1 h. The cooled reaction mixture was evaporated to dryness, dissolved in dichloromethane (100 ml), washed with dilute hydrochloric acid (3×50 ml) and water (50 ml), dried over anhydrous magnesium sulphate, filtered, and evaporated to give 5-acetamido-3-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole (5.3 g), m.p. 180-187° C., in the form of a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372774B1
Source datasetuspto-grants-2002_04
ORD IDord-343ed9ec598048c782e713f7a29a8dea
Source noteuspto-grants-2002_04