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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398462Generated: October 26, 2026

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

https://huagongshe.com/reaction/2398462

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 numberUS04024273
Source datasetuspto-grants-1977_05
ORD IDord-5c177075ef0d451a8ed724444b46b474
Source noteuspto-grants-1977_05