Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083229Generated: November 1, 2026

Hydrochloric Acid → 6-(1-Hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile

https://huagongshe.com/reaction/2083229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Cyano-4-oxo-4H-1-benzopyran-6-yl)ethyl acetateHCID 20358220—
Product6-(1-Hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrileHCID 13601325—

Reaction Steps

A mixture of 1.43 parts of 6-(1-acetoxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile and 25 parts by volume of 1N-sodium hydroxide is stirred at room temperature for 80 minutes. After being acidified with 1N-hydrochloric acid, the reaction mixture is extracted with ethyl acetate. The ethyl acetate layer is washed with water and dried on Na2SO4. The ethyl acetate is distilled off and the resulting residue is recrystallized from ethyl acetate. The procedure yields 0.790 part of 6-(1-hydroxyethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile as colorless crystals. Melting point: 147°-148° C

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085116
Source datasetuspto-grants-1978_04
ORD IDord-c05b85cbfad3416685ecc796ca9bc821
Source noteuspto-grants-1978_04