Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 5-Methylnicotinonitrile | HCID 637838 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 10329892 | HCID 10329892 | — |
Reaction Steps
3-Cyano-5-methylpyridine (2 g, 16.9 mmol) was dissolved in 1-propanol (100 ml). Sodium methoxide (46 mg, 0.85 mmol) was added, and the resulting mixture was stirred at 0° C. for 20 hours. After the completion of the reaction, the reaction mixture was neutralized with acetic acid (56 mg, 0.93 mmol), and the resulting mixture was concentrated under reduced pressure. After concentration, ethyl ether (50 ml) was added to the residue, and insoluble sodium acetate was removed by filtration. The filtrate was concentrated under reduced pressure to give a crude product of propyl 5-methyl-3-pyridinecarboximidate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05508293 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-dcae75bf85fb48e7928c6560b9a4e6b8 |
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| Source note | uspto-grants-1996_04 |
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