HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Methyl 5-amino-o-anisate | HCID 89843 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-Methoxy-3-(methoxycarbonyl)phenyl]ethanimidic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211199B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-ceb4242dc9cb476e92066dd0b5a8b12c |
| Source note | uspto-grants-2001_04 |