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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045457Generated: October 30, 2026

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

https://huagongshe.com/reaction/2045457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 3-amino-5-fluorobenzoateHCID 3807862—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product3-[(3-Bromo-benzylidene)-amino]-5-fluoro-benzoic acid methyl esterHCID 67439984100%

Reaction Steps

A mixture solution of 3-amino-5-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 3-[(3-bromo-benzylidene)-amino]-5-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 numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-f7b51957a9614b19a580af2c53f10440
Source noteuspto-grants-2013_11