Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542885Generated: October 30, 2026

Ethanol → 2-(5-Bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroethene

https://huagongshe.com/reaction/542885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantEthyl 3-ethoxy-2-nitroprop-2-enoateHCID 54104329—
SolventTolueneHCID 1140—
Product2-(5-Bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroetheneHCID 8674143063.2%

Reaction Steps

A mixture of 2-ethoxy-1-ethoxycarbonyl-1-nitroethene (5.7 g) and 2-amino-5-bromopyridine (5.2 g) in toluene was heated at reflux with slow removal of the ethanol formed during 2 hours. The reaction mixture was cooled and concentrated in vacuo to give a yellow powder which was triturated with hot ethanol, to give 2-(5-bromopyrid-2-ylamino)-1-ethoxycarbonyl-1-nitroethene (6.0 g) in the form of a pale yellow powder, m.p. 141°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659727
Source datasetuspto-grants-1987_04
ORD IDord-c3a8d47b0aba487a8228d03f5c3e5321
Source noteuspto-grants-1987_04