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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856906Generated: October 30, 2026

3-Hydroxybenzaldehyde → 3(2H)-Benzofuranone, 6-hydroxy-2-[(3-hydroxyphenyl)methylene]-

https://huagongshe.com/reaction/1856906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant6-Hydroxy-3-coumaranoneHCID 235717—
SolventMethanolHCID 887—
Product3(2H)-Benzofuranone, 6-hydroxy-2-[(3-hydroxyphenyl)methylene]-HCID 49005970.9%

Reaction Steps

After 6-hydroxy-2H-benzofuran-3-one 1 g and 3-hydroxybenzaldehyde 0.813 g were dissolved in methanol 75 ml, concentrated hydrochloric acid 50 ml was added, and the mixture was refluxed for two hours. The solution was cooled to room temperature, water 400 ml was added and allowed to stand for one hour. Precipitated crystals were filtered. The crystals were dried over phosphorous pentoxide at a temperature of 60° C. for five hours under reduced pressure to obtain the desired compound 1.20 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143779
Source datasetuspto-grants-2000_11
ORD IDord-1fd35ca8fae141c3a5cac3f5fd0cbf6d
Source noteuspto-grants-2000_11