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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045370Generated: October 30, 2026

3-Bromobenzaldehyde → HCID 67442776, compound

https://huagongshe.com/reaction/2045370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
ProductHCID 67442776HCID 6744277699.7%

Reaction Steps

A mixture solution of 5-amino-2-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 5-[(3-bromo-benzylidene)-amino]-2-chloro-benzoic acid methyl ester (39.8 g, quant.) as a pale-white solid: MS calcd. for C18H11BrClNO2 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-15ede68c6a91484ba8fa920961c4b471
Source noteuspto-grants-2013_11