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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607274Generated: October 31, 2026

2-(p-Methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuran → 2-(p-Methoxybenzyl)-3-methyl-4-hydroxy-5-propylbenzofuran

https://huagongshe.com/reaction/1607274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(p-Methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuranHCID 14579792—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(p-Methoxybenzyl)-3-methyl-4-hydroxy-5-propylbenzofuranHCID 14570889—

Reaction Steps

A solution of 2-(p-methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuran (40 mg) in ethanol (50 mL) was hydrogenated in a Parr hydrogenator in the presence of 10% palladium on charcoal at 40 psi. The catalyst was filtered and the filtrate was concentrated to dryness to yield 2-(p-methoxybenzyl)-3-methyl-4-hydroxy-5-propylbenzofuran, identical to the product prepared by the route described in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-668f860e16334c93b87debd5baa4288d
Source noteuspto-grants-1989_09