HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45238Generated: October 28, 2026
Ammonium Chloride → 5-(Hydroxymethyl)nicotinonitrile
https://huagongshe.com/reaction/45238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (5-Bromo-3-pyridinyl)methanol | HCID 2784733 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-(Hydroxymethyl)nicotinonitrile | HCID 22416540 | 71.1% |
Reaction Steps
A mixture of 4.2 g (22.34 mmol) of (5-bromopyridin-3-yl)methanol and 5 g (55.84 mmol) of copper cyanide in 22 mL of pyridine is heated for 20 hours in a sealed tube at 160° C. After cooling to room temperature, the medium is taken up in 10 mL of concentrated aqueous ammonia and 30 mL of saturated NH4Cl solution and then stirred for 2 hours. The medium is then extracted with 200 mL of a DCM/iPrOH mixture (85/15), dried over Na2SO4 and then concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with a 98/2 DCM/MeOH mixture. 2.13 g of 5-(hydroxymethyl)pyridine-3-carbonitrile are obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541455B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-e2beaf72d4444e209b36f2cd86514448 |
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| Source note | uspto-grants-2013_09 |
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