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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349467Generated: October 26, 2026

p-Toluenesulfonic acid → 4-methoxy-3-[(N-chloro-benzimidoyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/349467

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantBenzonitrileHCID 7505—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-Amino-4-methoxybenzoateHCID 2734814—
ReactantSodium HypochloriteHCID 23665760—
Product4-methoxy-3-[(N-chloro-benzimidoyl)-amino]-benzoic acid methyl esterHCID 6911957488%

Reaction Conditions

Temperature180 °C

Reaction Steps

Anhydrous p-toluene sulfonic acid (41.99 g, 220.8 mmol) was melted at 120° C. and 3-amino-4-methoxy benzoic acid methyl ester (20 g, 110.38 mmol) obtained in step 1 and benzonitrile (22.77 g, 220.8 mmol) were added thereto and stirred at 180° C. for 5 hours. The resulting solution was cooled to room temperature and the reaction was stopped by adding NaHCO3 thereto. The resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The concentrate was dissolved in 50% methanol and 5% NaOCl (56 Ml, 37.65 mmol) was added dropwise thereto. After 5 min, the resulting mixture was extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent—MeOH/CDCl3=5:95, Merck, Silicagel 60) to obtain the title compound (31 g, 25.10 mmol) in a yield of 88%;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179832B2
Source datasetuspto-grants-2007_02
ORD IDord-355faa56b66949f6b215a49bf9a90720
Source noteuspto-grants-2007_02