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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607276Generated: October 31, 2026

4-Bromobenzoyl chloride → HCID 15029669, compound

https://huagongshe.com/reaction/1607276

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% ethylacetate 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 numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-7a3e44f2e7124e3f891b2cd329a9fb4c
Source noteuspto-grants-1989_09