Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | HCID 19734534 | HCID 19734534 | — |
Reaction Steps
4-cyanopyridine (10.0 g, 96.1 mmol) was dissolved in isopropanol (50 ml), and sodium hydride (0.23 g, 9.6 mmol) from which oily matters had been removed by washing with ether was added. The mixture was stirred at room temperature for 6 hours. After the reaction was completed, the reaction solution was neutralized by adding acetic acid (0.64 g, 10.7 mmol) and concentrated under reduced pressure. To the residual concentrate was added diethyl ether (50 ml). Insolubles were removed by filtration, and the filtrate was concentrated under reduced pressure. To this concentrate was added hexane (80 ml), and deposited unreacted 4-cyanopyridine was removed by filtration. The filtrate was concentrated under reduced pressure to give crude isopropyl 4-pyridinecarboximidate (11.0 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05272164 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-f868d4f69ba44ee2a53d0a5f006c8c3b |
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| Source note | uspto-grants-1993_12 |
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