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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349501Generated: October 26, 2026

p-Toluenesulfonic acid → HCID 178498286, compound

https://huagongshe.com/reaction/349501

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-NitrobenzonitrileHCID 12090—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-Amino-4-methoxybenzoateHCID 2734814—
SolventBenzeneHCID 241—
ProductHCID 178498286HCID 17849828652%

Reaction Conditions

Temperature160 °C

Reaction Steps

Anhydrous p-toluenesulfonic acid (6.30 g, 33.1 mmol) was added to 50 ml of benzene and the resulting mixture was refluxed while removing water using a dean-stock trap. Added thereto were 3-amino-4-methoxy benzoic acid methyl ester (3 g, 16.6 mmol) obtained in step 1 of Preparation Example 1 and 4-nitrobenzonitrile (2.94 g, 19.9 mol), followed by stirring at 160° C. for 8 hours. The resulting solution was cooled to room temperature, the reaction was stopped by adding NaHCO3 thereto, 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 to obtain the title compound (2.83 g, 8.59 mmol) in a yield of 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179832B2
Source datasetuspto-grants-2007_02
ORD IDord-f8eccf94540f43b9aff3eaedff7b2137
Source noteuspto-grants-2007_02