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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637593Generated: October 26, 2026

Benzyl Bromide → 4-(2,4-Dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole

https://huagongshe.com/reaction/637593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
ReactantHCID 178481842HCID 178481842—
SolventBenzeneHCID 241—
Product4-(2,4-Dichlorobenzoyl)-1-methyl-5-benzyloxypyrazoleHCID 1332171393%

Reaction Steps

To a mixture of 1.50 g (0.0055 mol) of 4-(2,4-dichlorobenzoyl)-1-methyl-5-hydroxypyrazole, 0.56 g (0.0055 mol) of triethylamine and 30 ml of benzene was added 1.03 g (0.0061 mol) of benzyl bromide and the resulting mixture was heated under reflux for 2 hours with stirring. After cooling, precipitated triethyl amine hydrobromide was filtered off. The filtrate was concentrated under reduced pressure and was subjected to column chromatography (silica gel, using ethyl acetate/benzene 1:3 as an eluent) to give 1.79 g of the title compound 4-(2,4-dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole (yield: 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04557753
Source datasetuspto-grants-1985_12
ORD IDord-93814bf7ece5461c8ceb234868deca12
Source noteuspto-grants-1985_12