Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794363Generated: November 4, 2026

Diethyl p-aminobenzylphosphonate → HCID 9867874, compound

https://huagongshe.com/reaction/1794363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl p-aminobenzylphosphonateHCID 88358—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 69560524HCID 69560524—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 9867874HCID 986787461%

Reaction Steps

A mixture of diethyl 4-aminobenzylphosphonate (0.83 g), (E)-3-(5-phenyl-4-isoxazolyl)propenoic acid (0.69 g), 1-hydroxy-1H-1,2,3-benzotriazole hydrate (0.54 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.65 g) and N,N-dimethylformamide (30 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-diethylphosphonomethylphenyl)-3-(5-phenyl-4-isoxazolyl)propenamide (0.86 g, yield 61%) 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: 173–174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-70647dd7cf2c42608290a10bcf14b1bb
Source noteuspto-grants-2006_04