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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534245Generated: November 4, 2026

4-Bromobenzoyl chloride → HCID 15029669, compound

https://huagongshe.com/reaction/1534245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzoyl chlorideHCID 68515—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 14579737HCID 14579737—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 15029669HCID 15029669—

Reaction Steps

A solution of p-bromobenzoyl chloride (1.1 gm; 5.0 mmoles) in ethylene dichloride (5 mL) was added slowly to a cooled suspension of aluminium chloride (3.3 gm; 25 mmoles) in ethylene dichloride (75 mL). After stirring for a period of 10 minutes, 3-methyl-4-hydroxy-5-propyl-7-chlorobenzofuran (0.95 gm; 4.2 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% ethyleneacetate in hexane to yield 260 mg gm of 2-(p-bromobenzoyl-3-methyl-4-(p-bromobenzoyloxy)-5-propyl-7-chlorobenzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087638
Source datasetuspto-grants-1992_02
ORD IDord-d48ba1d3fb3542cca549f9ea8d544f9e
Source noteuspto-grants-1992_02