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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738704Generated: October 25, 2026

Potassium Hydroxide → 5-Bromo-2-(4-methoxybenzyl)benzofuran

https://huagongshe.com/reaction/1738704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-2-(4-methoxybenzoyl)benzofuranHCID 2371724—
ReactantHydrazine--water (1/2)HCID 22141362—
SolventDiethylene GlycolHCID 8117—
Product5-Bromo-2-(4-methoxybenzyl)benzofuranHCID 2184437082.5%

Reaction Steps

5.07 g of potassium hydroxide was added to 30 ml of diethylene glycol, and the mixture was stirred at room temperature during which 5.5 g of 80% hydrazine dihydrate.2H2O and 5.0 g of 5-bromo-2-(4-methoxybenzoyl)-benzofuran were further added. The thus prepared mixture was refluxed under heating. After cooling, the resulting reaction solution was adjusted to pH 4-5, extracted with benzene, and then dried. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a n-hexane/isopropanol mixture as an elution solvent, thereby obtaining 3.95 g of 5-bromo-2-(4-methoxybenzyl)benzofuran as a brown oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962695
Source datasetuspto-grants-1999_10
ORD IDord-eed1ef42a22940278fa467e9ff0405c0
Source noteuspto-grants-1999_10