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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482044Generated: October 30, 2026

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

https://huagongshe.com/reaction/482044

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 (25 g) and 25.2 g of pyridine were dissolved in 200 ml of dichloromethane and, with ice cooling, 33.3 g of phenyl chloroformate was added dropwise thereinto. The reaction solution was stirred with ice cooling for 30 minutes, washed with water and dried. The solvent was distilled off to give a mixture of phenyl 2,4-difluorophenylcarbamate and pyridine. To the mixture was added 30.7 g of 2-(diethoxy)ethylamine, and the resulting mixture was stirred at room temperature. The crystals separated out were collected by filtration 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 numberUS05792780
Source datasetuspto-grants-1998_08
ORD IDord-648134d0e1e04ea7aec0bf4feb4a5a2f
Source noteuspto-grants-1998_08