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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801104Generated: October 26, 2026

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

https://huagongshe.com/reaction/1801104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 2-amino-5-chlorobenzoateHCID 78878—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl esterHCID 6744257599.7%

Reaction Steps

A mixture solution of 2-amino-5-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 2-[(3-bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl ester (39.8 g, quant.) as a pale-white solid: MS calcd. for C15H11BrClNO2353.62, 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-72c0fc6a94444dd9b6ac73a96cdfaa85
Source noteuspto-grants-2013_01