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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801160Generated: November 1, 2026

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

https://huagongshe.com/reaction/1801160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 5-amino-2-fluorobenzoateHCID 15621043—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product5-[(3-Bromo-benzylidene)-amino]-2-fluoro-benzoic acid methyl esterHCID 67441633100%

Reaction Steps

A mixture solution of 5-amino-2-fluoro-benzoic acid methyl ester (26 g, 153.8 mmol), 3-bromo-benzaldehyde (28.5 g, 153.8 mmol) and p-toluenesulfonic acid (590 mg, 3.2 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-fluoro-benzoic acid methyl ester (51.7 g, quant.) as a pale-white solid: MS calcd. for C15H11BrFlNO2 337.16, obsd. (ESI+) [(M+H)+] 336.0 & 338.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-cf1981252f864bc6a887ba09d0b3714b
Source noteuspto-grants-2013_01