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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637185Generated: October 30, 2026

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

https://huagongshe.com/reaction/637185

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 numberUS06194406B1
Source datasetuspto-grants-2001_02
ORD IDord-6535b754317644fd9af2e66c534ab09d
Source noteuspto-grants-2001_02