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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229495Generated: October 30, 2026

Benzoic Acid → N-Benzoyl-L-tyrosine ethyl ester

https://huagongshe.com/reaction/2229495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantL-Tyrosine ethyl esterHCID 70364—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDimethylformamideHCID 6228—
ProductN-Benzoyl-L-tyrosine ethyl esterHCID 77033—

Reaction Steps

L-Tyrosine ethyl ester (0.28 g, 1.35 mmol) was dissolved in DMF (9 mL). Benzoic acid (1 eq, 1.35 mmol, 0.17 g) was added, followed by N-methylmorpholine (3 eq, 4.06 mmol, 0.45 mL), 1-hydroxybenzotriazole hydrate (1.2 eq, 1.62 mmol, 0.22 g), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (1.2 eq, 1.62 mmol, 0.31 g). The yellow solution was allowed to stir at room temperature under nitrogen for three days. The DMF was then removed by rotary evaporation and the resulting residue partitioned between ethyl acetate and water. The organic portion was separated and washed 3×H2O and 1×aq. saturated NaHCO3. It was dried over MgSO4, filtered, and concentrated to an oil. Trituration with diethyl ether induced formation of a white powder (0.32 g, 76%). MS (ES+) m/e 314 [M+H]+, 627.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420424B1
Source datasetuspto-grants-2002_07
ORD IDord-82f2a0a79c324a7893b05937fa07bf75
Source noteuspto-grants-2002_07