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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607267Generated: October 31, 2026

p-Anisoyl chloride → HCID 14579747, compound

https://huagongshe.com/reaction/1607267

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 14579736HCID 14579736—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 14579747HCID 1457974765.2%

Reaction Steps

A solution of p-anisoyl chloride (2.70 gm; 15.5mmoles) in ethylene dichloride (10 mL) was added slowly to a cooled suspension of aluminium chloride (3.0 gm; 21.8mmoles) in ethylene dichloride (100 mL). After stirring for a period of 10 minutes, 3-methyl-4-hydroxy-5-propyl-7-fluorobenzofuran (0.79 gm; 3.8mmoles) in dichloroethylene (5 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 agueous 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-(p-methoxybenzoyl)-3-methyl-4-(p-methoxybenzoyloxy)-5-propyl-7-fluorobenzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-5e6d876e766b468ea40c142ea8c4bf6d
Source noteuspto-grants-1989_09