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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349476Generated: October 23, 2026

p-Toluenesulfonic acid → HCID 69119733, compound

https://huagongshe.com/en/reaction/349476

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,4-DichlorobenzonitrileHCID 81050—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-Amino-4-methoxybenzoateHCID 2734814—
ReactantSodium HypochloriteHCID 23665760—
ProductHCID 69119733HCID 6911973384%

Reaction Conditions

Temperature180 °C

Reaction Steps

Anhydrous p-toluene sulfonic acid (20.99 g, 110.04 mmol) was melted at 120° C. and 3-amino-4-methoxy benzoic acid methyl ester (10 g, 55.20 mmol) obtained in step 1 of Preparation Example 1 and 2,4-dichlorobenzonitrile (18.99 g, 110.04 mol) were added thereto and stirred at 180° C. for 6 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 (30 ml, 20.64 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 (18 g, 10.32 mmol) in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179832B2
Source datasetuspto-grants-2007_02
ORD IDord-3577b128423d43f1b30b6d9e0ebc0a93
Source noteuspto-grants-2007_02