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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909694Generated: October 26, 2026

Ethanol → 2-Hydroxy-3',4'-dihydroxyacetophenone

https://huagongshe.com/reaction/909694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Chloro-3',4'-dihydroxyacetophenoneHCID 66834—
ReactantSodium FormateHCID 2723810—
SolventFormic AcidHCID 284—
SolventWaterHCID 962—
Product2-Hydroxy-3',4'-dihydroxyacetophenoneHCID 2213444482.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 1 liter reactor equipped with a reflux condenser and magnetic stirring bar was charged under argon with 45 g of 4-chloroacetyl-catechol of a purity of ca. 90%, 260 ml of ethanol, 130 ml of water, 38 g of sodium formate and 17 ml (˜21 g) of formic acid. The stirred mixture was heated under reflux (˜100° C.) for 24 hours. Under vacuum a part of the solvents was distilled off. The remaining solution of about 100 ml was acidified by addition of 35.5 g of conc. hydrochloric acid (37%) resulting in a pH of about 0.5. 200 ml of water were added and the mixture was refluxed for 10 minutes. Upon stirring over night without heating crystals separated. The slurry was filtered by suction and the crystals were washed with 50 ml of cold water. After drying over night at 70° C. at ˜20 mbar the yield of 4-hydroxyacetyl-catechol was 34.2 g with a purity of 89.2% corresponding to a yield of 82.6%. In the mother liquors additional 14% of the product was detected by analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017815B2
Source datasetuspto-grants-2011_09
ORD IDord-18f75289afee420e8f3c495c8826ed20
Source noteuspto-grants-2011_09