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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801137Generated: October 31, 2026

3-Bromobenzaldehyde → 4-[(3-Bromo-benzylidene)-amino]-3-chloro-benzoic acid methyl ester

https://huagongshe.com/reaction/1801137

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 4-Amino-3-chlorobenzoateHCID 1515284—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product4-[(3-Bromo-benzylidene)-amino]-3-chloro-benzoic acid methyl esterHCID 6744173599.7%

Reaction Steps

A mixture solution of 4-amino-3-chloro-benzoic acid methyl ester (21 g, 113.2 mmol), 3-bromo-benzaldehyde (21 g, 113.2 mmol) and p-toluenesulfonic acid (431 mg, 2.2 mmol) in toluene (200 mL) was heated to reflux for 12 hours. Then the reaction mixture was cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 4-[(3-bromo-benzylidene)-amino]-3-chloro-benzoic acid methyl ester (39.8 g, quant.) as a pale-white solid: MS calcd. for C15H11BrClNO2 353.62, obsd. (ESI+) [(M+H)+] 351.9 & 353.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-ff8e262193cb47d1997d16c30df349cb
Source noteuspto-grants-2013_01