HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1071777Erstellt: 23. Oktober 2026
(+-)-4-Hydroxymandelic acid → Benzeneacetic acid, alpha,4-dihydroxy-, ethyl ester
https://huagongshe.com/de/reaction/1071777
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Benzeneacetic acid, alpha,4-dihydroxy-, ethyl ester | HCID 111357 | 288% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06906113B2 |
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| Quelldatensatz | uspto-grants-2005_06 |
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| ORD ID | ord-483957f9c4454e988f199e2119f4489a |
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| Quellennotiz | uspto-grants-2005_06 |
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