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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913755Generated: November 1, 2026

Benzyl Alcohol → 3-(Benzyloxy)pyridine-4-carbonitrile

https://huagongshe.com/reaction/1913755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloropyridine-4-carbonitrileHCID 10678306—
SolventDimethylformamideHCID 6228—
Product3-(Benzyloxy)pyridine-4-carbonitrileHCID 1082234187%

Reaction Steps

A mixture of 0.59 g of 60% sodium hydride (in oil) and 5 ml of DMF was stirred while ice-cooling. To the reaction mixture, 1.59 g of benzyl alcohol was added. The reaction mixture was stirred at the same temperature for 10 minutes. To the reaction mixture, 2.0 g of 3-chloroisonicotinonitrile was added, and the reaction mixture was stirred at the same temperature for 30 minutes and at room temperature for 1.5 hours. The reaction mixture was concentrated under reduced pressure, and then to ethyl acetate was added to the reaction mixture, followed by filtration of insoluble matters. The filtrate was concentrated under reduced pressure and the resultant residue was subjected to silica gel column chromatography to give 2.64 g of 3-benzyloxy isonicotinonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609705B2
Source datasetuspto-grants-2013_12
ORD IDord-70f7effa65094ba6b4afd49b1700766e
Source noteuspto-grants-2013_12