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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133672Generated: October 26, 2026

Hydrochloric Acid → 4-Hydroxy-4-(4-hydroxyphenylmethyl)-2-hydroxyiminoglutaric acid

https://huagongshe.com/reaction/133672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxaloacetic AcidHCID 970—
Reactant4-Hydroxyphenylpyruvic AcidHCID 979—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
Product4-Hydroxy-4-(4-hydroxyphenylmethyl)-2-hydroxyiminoglutaric acidHCID 86595817—

Reaction Steps

To 10 ml of water in which were dissolved 3.18 g of potassium hydroxide, were added 1.0 g (5.55 mmol) of 4-hydroxyphenylpyruvic acid and 2.2 g (16.7 mmol) of oxalacetic acid, for reaction at ambient temperature for 72 hours (about pH 13 at the start of the reaction). Hydroxylamine hydrochloride salt of 1.54 g (22.2 mmol) was added to the reaction solution, for reaction at ambient temperature for 10 hours. The reaction solution was then adjusted to pH 2.6, using 6N hydrochloric acid, for extraction using ethyl acetate. The organic layer was rinsed with aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate and concentrated to dryness, to obtain 0.7 g (2.47 mmol) of 4-hydroxy-4-(4-hydroxyphenylmethyl)-2-hydroxyiminoglutaric acid as a crude product. Further, the crude product was recrystallized in methanol and toluene, to obtain 0.22 g (0.78 mmol) of 4-hydroxy-4-(4-hydroxyphenylmethyl)-2-hydroxyiminoglutaric acid in crystal. NMR Measurement

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390909B2
Source datasetuspto-grants-2008_06
ORD IDord-c32f370aec4a4a6ca019a493a8337590
Source noteuspto-grants-2008_06