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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzeneacetic acid, alpha,4-dihydroxy-, ethyl ester | HCID 111357 | 288% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06906113B2 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-483957f9c4454e988f199e2119f4489a |
|---|
| Source note | uspto-grants-2005_06 |
|---|