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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238315Generated: October 27, 2026

Triethylamine → Phenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamate

https://huagongshe.com/reaction/238315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-(4-Fluoro-2-nitrophenoxy)propylamineHCID 62348405—
Solvent1,4-DioxaneHCID 31275—
ProductPhenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamateHCID 8664193494.2%

Reaction Steps

Triethylamine (2.90 ml, 21.4 mmol) and phenyl chlorocarbonate (2.52 ml, 20.0 mmol) were added to a dioxane solution (43 ml) of 3-(4-fluoro-2-nitrophenoxy)propylamine (4.03 g, 18.8 mmol), while being cooled with ice, and the mixture was stirred at room temperature for 0.5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (dichloromethane:ethyl acetate=30:1). The purified product was concentrated to dryness under reduced pressure to thereby obtain 5.92 g of powdery yellow phenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamate (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642619B2
Source datasetuspto-grants-2014_02
ORD IDord-ec5108af1df542c88c0e0d3b2918c4fe
Source noteuspto-grants-2014_02