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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071777Generated: October 26, 2026

(+-)-4-Hydroxymandelic acid → Benzeneacetic acid, alpha,4-dihydroxy-, ethyl ester

https://huagongshe.com/reaction/1071777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-4-Hydroxymandelic acidHCID 328—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductBenzeneacetic acid, alpha,4-dihydroxy-, ethyl esterHCID 111357288%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 5 g of 4-hydroxymandelic acid and 1.28 g of p-toluenesulfonic acid in 200 ml of ethanol is heated at 50° C. for 4 hours. The mixture is poured into saturated aqueous NaHCO3 solution, and a white precipitate is formed. The mixture is diluted with water until the precipitate disintegrates, and then is extracted with diethyl ether. The organic phases are dried over sodium sulfate. Filtration and evaporation of the solvent give ethyl 4-hydroxymandelate (4.2 g, 82%) as a pale yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906113B2
Source datasetuspto-grants-2005_06
ORD IDord-483957f9c4454e988f199e2119f4489a
Source noteuspto-grants-2005_06