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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045491Generated: October 30, 2026

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

https://huagongshe.com/reaction/2045491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 3-amino-5-chlorobenzoateHCID 52987785—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product3-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl esterHCID 6744279599.7%

Reaction Steps

A mixture solution of 3-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 3-[(3-bromo-benzylidene)-amino]-5-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 numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-0fd7e7d7d1cc463a89782b89830f53c9
Source noteuspto-grants-2013_11