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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129157Generated: October 29, 2026

Pyridine → N-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)urea

https://huagongshe.com/reaction/129157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,4-DifluoroanilineHCID 9709—
ReactantPhenyl chloroformateHCID 15891—
Reactantphenyl N-(2,4-difluorophenyl)carbamateHCID 13733129—
SolventDichloromethaneHCID 6344—
ProductN-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)ureaHCID 19065111—

Reaction Steps

2,4-difluoroaniline (25g) and 25.2 g of pyridine were dissolved in 200 ml of dichloromethane to which was added dropwise 33.3 g of phenyl chloroformate with ice cooling. After stirring for 30 minutes with ice cooling, the reaction solution was washed with water and dried followed by distilling the solvent to give a mixture of phenyl 2,4-difluorophenylcarbamate and pyridine. To the mixture was added 30.7 g of 2-(di-ethoxy)ethylamine and the mixture was stirred at room temperature. The crystals separated out were filtered and washed with petroleum ether to give 37.8 g of N-(2,2-diethoxyethyl)-N'-(2,4-difluorophenyl)urea as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466820
Source datasetuspto-grants-1995_11
ORD IDord-458278adf92941f1a13d84297af8e95b
Source noteuspto-grants-1995_11