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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459113Generated: October 26, 2026

Hydrochloric Acid → 2,4-Bis-(4-hydroxybenzyl)-3-azaglutaric acid-diisopropyl ester

https://huagongshe.com/reaction/1459113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Hydroxyphenylpyruvic AcidHCID 979—
ReactantL-TyrosineHCID 6057—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2,4-Bis-(4-hydroxybenzyl)-3-azaglutaric acid-diisopropyl esterHCID 54124893—

Reaction Conditions

Temperature60 °C

Reaction Steps

9.01 g (50.0 mmol) of 4-hydroxyphenylpyruvic acid and 9.06 g (50.0 mmol) of tyrosine are dissolved in 60 ml of methanol and stirred for six hours at 60° C. Then, it is allowed to cool to room temperature and 0.76 g (20 mmol) of sodium borohydride is added. It is allowed to stir overnight and then the reaction mixture is mixed carefully with diluted hydrochloric acid until no more gas generation can be observed. The reaction mixture is concentrated by evaporation and dried in an oil pump vacuum for several hours at 100° C. The residue is taken up in isopropanol. Hydrogen chloride gas is introduced until saturation is achieved, stirred for two hours at room temperature and then for eight hours at 85° C. Then, it is concentrated by evaporation, the residue is dispersed between ethyl acetate and sodium bicarbonate solution, the organic phase is dried on sodium sulfate, filtered and concentrated by evaporation. The residue is chromatographed on silica gel with use of hexane/ethyl acetate as mobile solvent. The fractions that contain the pure product are combined and concentrated by evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853699
Source datasetuspto-grants-1998_12
ORD IDord-7cf6e1c10daa4481929a646a6cf9d50d
Source noteuspto-grants-1998_12