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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268362Generated: October 27, 2026

p-Anisoyl chloride → 3-(4-Hydroxybenzoyl)-2-(4-tolyl)benzofuran

https://huagongshe.com/reaction/268362

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
Reactant2-(p-Tolyl)benzofuranHCID 638458—
Reactant3-(4-Methoxybenzoyl)-2-(4-tolyl)benzofuranHCID 21435289—
Product3-(4-Hydroxybenzoyl)-2-(4-tolyl)benzofuranHCID 21435268—

Reaction Steps

3-(4-Hydroxybenzoyl)-2-(4-tolyl)benzofuran is prepared by acylation of 2-(4-tolyl)benzofuran with p-anisoyl chloride followed by demethylation of the 3-(4-methoxybenzoyl)-2-(4-tolyl)benzofuran thus formed as described in the procedure of Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947470
Source datasetuspto-grants-1976_03
ORD IDord-53fdcf57bb334061a2bcf6cc6a979e9a
Source noteuspto-grants-1976_03