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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801146Generated: October 31, 2026

Benzocaine → 4-[(5-Bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl ester

https://huagongshe.com/reaction/1801146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product4-[(5-Bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl esterHCID 67440476101.4%

Reaction Steps

A mixture of 4-amino-benzoic acid ethyl ester (16.5 g, 100 mmol), 5-bromo-pyridine-3-carbaldehyde (18.6 g, 100 mmol) and p-toluenesulfonic acid (380 mg, 2 mmol) in toluene (200 mL) was heated to reflux for 12 h. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 4-[(5-bromo-pyridin-3-ylmethylene)-amino]-benzoic acid ethyl ester (33.8 g, quant.) as a light yellow solid: LC/MS m/e calcd for C15H13BrN2O2 (M+H)+: 334.19, observed: 332.9 & 335.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-9563873ab8324b68a663da47cbb3bb2a
Source noteuspto-grants-2013_01