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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107864Generated: October 30, 2026

Hydrochloric Acid → 3-Methyl-6-hydroxybenzofuran

https://huagongshe.com/reaction/1107864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant(3-Hydroxyphenoxy)acetoneHCID 18786125—
Product3-Methyl-6-hydroxybenzofuranHCID 1085562460.4%

Reaction Conditions

Temperature5 °C

Reaction Steps

3 g (18 mmol) of (3-hydroxyphenoxy)acetone and 400 ml of a 0.1M potassium hydroxide solution are introduced into a 1 l three-necked flask equipped with a reflux condenser. Heating is carried out at reflux for 6 hours. The reaction mixture is cooled to 5° C., a molar hydrochloric acid solution is added, in order to obtain a pH of approximately 5, and extraction is carried out with ethyl ether (3×150 ml). The organic phases are combined, dried over magnesium sulphate and concentrated. The residue is purified by silica column chromatography (elution solvent: 8/2 cyclohexane/ethyl acetate). 1.61 g of 3-methyl-6-hydroxybenzofuran are obtained--M.p.: 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063810
Source datasetuspto-grants-2000_05
ORD IDord-80cae4e0f7424c6ea2f4512a170fc7a7
Source noteuspto-grants-2000_05