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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534243Generated: November 1, 2026

Benzoyl chloride → HCID 14579772, compound

https://huagongshe.com/reaction/1534243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 14579737HCID 14579737—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 14579772HCID 1457977263%

Reaction Steps

A solution of benzoyl chloride (3.03 gm; 21.6 mmoles) in ethylene dichloride (20 mL) was added slowly to a cooled suspension of aluminium chloride (5.8 gm; 43 mmoles) in ethylenedichloride (100 mL). After stirring for a period of 10 minutes, 3-methyl-4-hydroxy-5-propyl-7-chlorobenzofuran (1.62 gm; 7.2 mmoles) in dichloroethylene (20 mL) was added over a period of 2 minutes. The reaction mixture was stirred at room temperature for 1 hour. It was cooled with an ice-bath and ice was added slowly. When the vigorous reaction subsided, the organic layer was separated and the aqueous phase was extracted with methylene chloride. The organic phases were combined, dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed on silica gel and eluted with 10% ethylacetate in hexane to yield 1.18 gm (63%) of 2-benzoyl-3-methyl-4-benzoyloxy-5-propyl-7-chlorobenzofuran, mp. 141°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087638
Source datasetuspto-grants-1992_02
ORD IDord-31bebce4d974437b88a9347cfc56bf8d
Source noteuspto-grants-1992_02