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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801082Generated: October 30, 2026

3-Bromobenzaldehyde → 2-{[1-(3-Bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl ester

https://huagongshe.com/reaction/1801082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMethyl 2-amino-5-fluorobenzoateHCID 2783401—
SolventEthanolHCID 702—
Product2-{[1-(3-Bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl esterHCID 6744143252%

Reaction Steps

A mixture of 2-amino-5-fluoro-benzoic acid methyl ester (15 g, 89 mmol) and 3-bromo-benzaldehyde (16.4 g, 89 mmol) in ethanol (200 mL) was heated to reflux for 2 hours. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 2-{[1-(3-bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl ester (15.3 g, 52%) as a white solid: LC/MS m/e calcd for C15H11BrFNO2 M+: 336.2, observed: 336.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-b932fd473d474baf90b7838f999ea9a7
Source noteuspto-grants-2013_01