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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloropyridine-4-carbonitrile | HCID 10678306 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Benzyloxy)pyridine-4-carbonitrile | HCID 10822341 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609705B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-70f7effa65094ba6b4afd49b1700766e |
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| Source note | uspto-grants-2013_12 |
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