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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856932Generated: October 30, 2026

Benzoyl chloride → HCID 54133674, compound

https://huagongshe.com/reaction/1856932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 53855529HCID 53855529—
SolventPyridineHCID 1049—
ProductHCID 54133674HCID 54133674—

Reaction Steps

After 2-[(3,5-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 ethyl acetate phase 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 and 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 388.5 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143779
Source datasetuspto-grants-2000_11
ORD IDord-31433ccdf58e40cbb71d86e5f8ce7e00
Source noteuspto-grants-2000_11