HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327098Generated: October 30, 2026
3-Cyanopyridine → HCID 10012236, compound
https://huagongshe.com/reaction/327098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Cyanopyridine | HCID 79 | — |
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | HCID 10012236 | HCID 10012236 | — |
Reaction Steps
3-cyanopyridine (10.0 g, 96.1 mmol) was dissolved in isopropanol (50 ml). Sodium hydride (0.23 g, 9.6 mmol) from which oily matters had been removed by washing with ether was added to the solution, and the mixture was stirred at room temperature for 3 hours. After the reaction was completed, acetic acid (0.64 g, 10.7 mmol) was added to neutralize the reaction solution, and the solution was concentrated under reduced pressure. After concentrating the solution, diethyl ether (80 ml) was added to the concentrated residue, and insoluble products were removed by filtration. The filtrate was concentrated under reduced pressure, and hexane (80 ml) was added to the concentrated residue, and depositing unreacted 3-cyanopyridine.was removed by filtration. The hexane solution was then concentrated under reduced pressure to give the crude product of isopropyl 3-pyridinecarboximidate as a pale yellow oil in a yield of 5.68 g.
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-c853fe59bbc243c393bfd58c9c61f872 |
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| Source note | uspto-grants-1993_12 |
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