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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859184Generated: November 2, 2026

Allyl bromide → HCID 58763935, compound

https://huagongshe.com/reaction/859184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantHCID 24828929HCID 24828929—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 58763935HCID 58763935—

Reaction Steps

To a slurry of sodium hydride (39 mg of 60% in oil) in DMSO (2.4 ml) was added 5-(4-chlorophenyl)-1-(2-chlorophenyl)-4-hydroxy-1H-pyrazole-3-carboxylic acid ethyl ester I-1d (300 mg, 0.8 mmol) and the mixture was agitated for 45 minutes. Allyl bromide (0.1 ml, 1.2 mmol) was added and stirring was continued for 4.5 hours. The reaction solution was diluted into ethyl acetate, washed with water (2×), brine, dried (Na2SO4) and concentrated in vacuo to afford the title compound (I-1e) as an orange oil, 340 mg. This material was taken onto the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151097B2
Source datasetuspto-grants-2006_12
ORD IDord-00aa5c030d9e423fbee44a1e4c42cfdf
Source noteuspto-grants-2006_12