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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504283Generated: October 31, 2026

Benzoyl chloride → HCID 67815312, compound

https://huagongshe.com/reaction/1504283

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 numberUS09212348B2
Source datasetuspto-grants-2015_12
ORD IDord-001785f2c041453b8890234d7c72a93b
Source noteuspto-grants-2015_12