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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794374Generated: October 25, 2026

Diethyl p-aminobenzylphosphonate → HCID 86591381, compound

https://huagongshe.com/reaction/1794374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl p-aminobenzylphosphonateHCID 88358—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5-Phenyl-4-isoxazolylacetic acidHCID 10035775—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86591381HCID 8659138189.2%

Reaction Steps

A mixture of diethyl 4-aminobenzylphosphonate (1.20 g), 5-phenyl-4-isoxazolylacetic acid (0.84 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (0.75 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.97 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 N-(4-diethylphosphonomethylphenyl)-5-phenyl-4-isoxazolylacetamide (1.58 g, yield 89%) 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: 132–133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-02432c018f484969b369124e9f306cad
Source noteuspto-grants-2006_04