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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230650Generated: October 30, 2026

Pyridine → N-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acid

https://huagongshe.com/reaction/2230650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantMethyl 5-amino-o-anisateHCID 89843—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acidHCID 4153338—

Reaction Steps

Combine methyl 2-methoxy-5-aminobenzoate (2.0 g, 11 mmol), pyridine, 2.8 mL, 35 mmol), and acetic anhydride (3.2 mL, 34 mmol) in tetrahydrofuran (50 mL). After 20 hours, concentrate the reaction mixture in vacuo to remove most of the tetrahydrofuran, partition between ethyl acetate and water. Separate the layers and extract the aqueous layer twice with ethyl acetate. Combine the organic layers, extract with brine, dry over MgSO4, filter, and evaporate in vacuo to give a residue. Crystallize the residue from ethyl acetate/cyclohexane to give methyl 2-methoxy-5-acetamidobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-b25e3e1868dd4df9b75c5a7aef3b8cae
Source noteuspto-grants-2002_07