Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085258Generated: October 26, 2026

Pyridine → N-(2-Bromoethyl)-p-nitrobenzamide

https://huagongshe.com/reaction/1085258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
SolventChloroformHCID 6212—
ProductN-(2-Bromoethyl)-p-nitrobenzamideHCID 458985—

Reaction Steps

In 30 ml of chloroform were added 3 g of 4-nitrobenzoyl chloride, 3.3 g of 2-aminoethyl bromide hydrobromide and 3.9 ml of pyridine under ice cooling, and they were stirred at the same temperature for 1 hour. The reaction mixture was then washed with water, and the resulting organic layer was concentrated to obtain a crude product of 2-(4-nitrobenzoylamino)ethyl bromide. Afterward, the latter was recrystallized from hexane/ethanol, the resulting crystals were collected by filtration, washed and dried to prepare 2.9 g of 2-(4-nitrobenzoylamino)ethyl bromide (compound 46).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008267
Source datasetuspto-grants-1991_04
ORD IDord-6552b384b67f4658950798dd857919fd
Source noteuspto-grants-1991_04