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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901058Generated: October 26, 2026

Diisopropylamine → Phenyl 4-fluoro-2-nitrophenylcarbamate

https://huagongshe.com/reaction/1901058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPhenyl chloroformateHCID 15891—
Reactant4-Fluoro-2-nitroanilineHCID 67769—
SolventDichloromethaneHCID 6344—
ProductPhenyl 4-fluoro-2-nitrophenylcarbamateHCID 2337007529.7%

Reaction Steps

To a solution of 4-fluoro-2-nitroaniline (1.56 g) and diisopropylamine (1.68 ml) in dichloromethane (20 ml) was added dropwise under ice-cooling phenyl chloroformate (1.51 g). After stirring the mixture at room temperature overnight, the reaction solution was washed with water, saturated saline, dried over anhydrous MgSO4 and the solvent was distilled off. Crystallization of the residue from diisopropyl ether afforded phenyl 4-fluoro-2-nitrophenylcarbamate (0.79 g, 29%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576335
Source datasetuspto-grants-1996_11
ORD IDord-4bb9718890f247318728fbcea8bc5ab7
Source noteuspto-grants-1996_11