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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244944Generated: October 30, 2026

Benzoyl chloride → HCID 67815312, compound

https://huagongshe.com/reaction/244944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 67811749HCID 67811749—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67815312HCID 6781531285%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromo-3-isopropyl-1-(2-methyl-1-phenylpropan-2-yl)-1H-pyrazol-5(4H)-one (3.00 g, 8.90 mmol) was dissolved in 39 mL of tetrahydrofuran and cooled with ice to 0° C., and after dropwise addition of 1.80 g (17.8 mmol) of triethylamine and 1.38 g (9.82 mmol) of benzoyl chloride, stirred at room temperature for 3 hours under a nitrogen atmosphere. The reaction was quenched with distilled water, and the reaction solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (silica gel 12 g, ethyl acetate:hexane=1:20) to give 3.34 g of the desired product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658686B2
Source datasetuspto-grants-2014_02
ORD IDord-3787d6a30bbf453fa0a6ba8df44c6adc
Source noteuspto-grants-2014_02