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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856931Generated: November 1, 2026

Benzoyl chloride → HCID 3825758, compound

https://huagongshe.com/reaction/1856931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 490061HCID 490061—
SolventPyridineHCID 1049—
ProductHCID 3825758HCID 3825758—

Reaction Steps

After 2-[(3,4-dimethoxyphenyl)methylene]-6-hydroxy-3(2H)-benzofuranone 0.5 g was dissolved in pyridine 5 ml, benzoyl chloride 0.282 ml was added, and the mixture was refluxed for two hours. The reaction mixture was cooled to room temperature, ethyl acetate 50 ml was added, and the mixture was washed with 2N-hydrochloric acid 50 ml twice and with saturated sodium bicarbonate solution 50 ml. After the ethyl acetate solution was dehydrated with anhydrous magnesium sulfate, it was concentrated under reduced pressure. The residue was fractionated by silica gel column chromatography (silica gel: 50 g, eluted with solvent 500 ml of hexane:ethyl acetate=1:1) and the fraction was concentrated to dryness at a temperature of 40° C. under reduced pressure to obtain crystals. The crystals were dried over phosphorous pentoxide at a temperature of 60° C. for four hours under reduced pressure to obtain the desired compound 294.6 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143779
Source datasetuspto-grants-2000_11
ORD IDord-cfcc3c37932440aaab44ead3c4ac7481
Source noteuspto-grants-2000_11