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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801054Generated: October 26, 2026

3-Bromobenzaldehyde → 2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl ester

https://huagongshe.com/reaction/1801054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 2-amino-5-chlorobenzoateHCID 78878—
SolventEthanolHCID 702—
Product2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl esterHCID 6744257524%

Reaction Steps

A mixture of 2-amino-5-chloro-benzoic acid methyl ester (11.7 g, 63 mmol) and 3-bromo-benzaldehyde (11.7 g, 63 mmol) in ethanol (200 mL). The reaction mixture was heated to reflux for 2 hours. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 2-{[1-(3-bromo-phenyl)-methylidene]-amino}-5-chloro-benzoic acid methyl ester (5.3 g, 24%) as a white solid: LC/MS m/e calcd for C15H11BrClNO2 M+: 353.6, observed: 353.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-9197ae25f9ff49c49518f9379e22e07f
Source noteuspto-grants-2013_01