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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350745Generated: October 25, 2026

Triethylamine → HCID 21088664, compound

https://huagongshe.com/reaction/350745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantDiethyl (4-aminophenyl)phosphonateHCID 273213—
ReactantHCID 21088670HCID 21088670—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21088664HCID 2108866436%

Reaction Steps

To a mixture of 4-(4-chlorophenyl)-2-phenyl-5-oxazolepropionic acid (500 mg), triethylamine (230 mg) and tetrahydrofuran (10 ml) was added ethyl chlorocarbonate (250 mg) at −40° C., and the mixture was stirred for 1 hr. Diethyl 4-aminophenylphosphonate (420 mg) was added, and the mixture was stirred at room temperature for 5 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography and 3-[4-(4-chlorophenyl)-2-phenyl-5-oxazolyl]-N-[4-(diethylphosphono)phenyl]propionamide (295 mg, yield 36%) was obtained as colorless prism crystals from a fraction eluted with ethyl acetate-chloroform (1:1, volume ratio). melting point: 139–140° C. (recrystallized from dichloromethane-isopropyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183276B2
Source datasetuspto-grants-2007_02
ORD IDord-80ed209e5d724ba0bae6bf557db3fb2a
Source noteuspto-grants-2007_02