Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607272Generated: October 31, 2026

Hydrazine → 2-(p-Methoxybenzyl)-3-methyl-4-hydroxybenzofuran

https://huagongshe.com/reaction/1607272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(p-Methoxybenzoyl)-3-methyl-4-hydroxybenzofuranHCID 14579791—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
Product2-(p-Methoxybenzyl)-3-methyl-4-hydroxybenzofuranHCID 1457088837,270.699%

Reaction Conditions

Temperature195 °C

Reaction Steps

A mixture of 2-(p-methoxybenzoyl)-3-methyl-4-hydroxybenzofuran (2.0 gm; 7.0 mmoles), 99% hydrazine (50 mL) and potassium hydroxide (2.7 gm; 49 mmoles) in ethylene glycol (50 mL) was heated at 140° C. for a period of 2.5 hours and at 195° C. for one hour. The reaction mixture was cooled, poured in water, and extracted with ethylacetate. The organic phase was washed with 20% citric acid, with brine, dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed on silica gel using 20% ethylacetate in hexane as eluent to yield 700 gm (37%) of 2-(p-methoxybenzyl)-3-methyl-4-hydroxybenzofuran, mp.130°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-0815bb20f2fb4256bb4ceff8fed4dff1
Source noteuspto-grants-1989_09