Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323452Generated: October 30, 2026

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

https://huagongshe.com/reaction/323452

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 aqueous layer 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 numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-ceb4242dc9cb476e92066dd0b5a8b12c
Source noteuspto-grants-2001_04