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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414432Generated: October 29, 2026

Triethylamine → N-[2-(2-ethoxyphenoxy)ethyl]-3-(4-fluorobenzoyl)-propionamide

https://huagongshe.com/reaction/1414432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-(4-Fluorobenzoyl)propionic acidHCID 101359—
Reactant2-(2-Ethoxyphenoxy)ethylamineHCID 5303042—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(2-ethoxyphenoxy)ethyl]-3-(4-fluorobenzoyl)-propionamideHCID 21487435—

Reaction Steps

To a stirred solution of 10.4 g of 3-(4-fluorobenzoyl)propionic acid and 6.0 g of triethylamine in 120 ml of tetrahydrofuran was added dropwise 6.0 g of ethyl chloroformate at a temperature below 0° C. After stirring was continued for half an hour, to the mixture was added a solution of 9.6 g of 2-(2-ethoxyphenoxy)ethylamine in 10 ml of tetrahydrofuran. Further stirring was continued at room temperature for 4 hours. The reaction mixture was filtered and the filtrate was concentrated to a residue under reduced pressure. The residue was recrystallized from benzene-hexane to give N-[2-(2-ethoxyphenoxy)ethyl]-3-(4-fluorobenzoyl)-propionamide melting at 98° - 100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001312
Source datasetuspto-grants-1977_01
ORD IDord-e78a834b8f654db5b659557e3d3e70a7
Source noteuspto-grants-1977_01