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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327098Generated: October 30, 2026

3-Cyanopyridine → HCID 10012236, compound

https://huagongshe.com/reaction/327098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-CyanopyridineHCID 79—
ReactantAcetic AcidHCID 176—
ReactantIsopropanolHCID 3776—
ReactantSodium hydrideHCID 24758—
ProductHCID 10012236HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272164
Source datasetuspto-grants-1993_12
ORD IDord-c853fe59bbc243c393bfd58c9c61f872
Source noteuspto-grants-1993_12