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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580261Generated: October 29, 2026

Allyl bromide → 1-(2-Fluoro-4-chloro-5-allyloxyphenyl)-3,4,5-trimethylpyrazole

https://huagongshe.com/reaction/580261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazoleHCID 13798233—
SolventAcetonitrileHCID 6342—
Product1-(2-Fluoro-4-chloro-5-allyloxyphenyl)-3,4,5-trimethylpyrazoleHCID 1379827397.3%

Reaction Steps

A mixture of 1-(2-fluoro-4-chloro-5-hydroxyphenyl)-3,4,5-trimethylpyrazole (25.5 g), allyl bromide (13.3 g), anhydrous potassium carbonate (14.5 g) and acetonitrile (150 ml) was heated under reflux, with stirring for 3 hours. After cooling, the reaction mixture was filtered through a filter to remove the inorganic salts therefrom and the filtrate was concentrated to a small volume under reduced pressure, affording the titled compound (28.7 g) as a pale brown crystalline solid. Recrystallization of this solid from cyclohexane yielded a white crystalline solid. m.p. 97°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752326
Source datasetuspto-grants-1988_06
ORD IDord-1d1d2e107bcd4aa8bc568ea5c96b3a86
Source noteuspto-grants-1988_06