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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794451Generated: October 31, 2026

p-Aminophenylacetic acid ethyl ester → HCID 69562013, compound

https://huagongshe.com/reaction/1794451

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 69561163HCID 69561163—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69562013HCID 69562013112.5%

Reaction Steps

A mixture of ethyl 4-aminophenylacetate (1.11 g), (E)-3-(3-methyl-5-phenyl-4-isoxazolyl)propenoic acid (0.95 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (0.75 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.91 g) and N,N-dimethylformamide (20 ml) was stirred at room temperature overnight. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate and then saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and (E)-N-(4-ethoxycarbonylmethylphenyl)-3-(3-methyl-5-phenyl-4-isoxazolyl)propenamide (1.82 g, yield 97%) was obtained as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). The crystals were recrystallized from ethyl acetate-hexane. melting point: 164–165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-b7c0d5135af5425fbc0209fa3bff4c3f
Source noteuspto-grants-2006_04