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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1801104Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1801104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromobenzaldehydeHCID 76583—
EduktMethyl 2-amino-5-chlorobenzoateHCID 78878—
Katalysatorp-Toluenesulfonic acidHCID 6101—
LösungsmittelTolueneHCID 1140—
Produkt2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl esterHCID 6744257599,7%

Reaktionsschritte

A mixture solution of 2-amino-5-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 2-[(3-bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl ester (39.8 g, quant.) as a pale-white solid: MS calcd. for C15H11BrClNO2353.62, obsd. (ESI+) [(M+H)+] 351.9 & 353.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08344137B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-72c0fc6a94444dd9b6ac73a96cdfaa85
Quellennotizuspto-grants-2013_01