Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | 2-Chloroisonicotinic acid | HCID 236985 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Chloropyridin-4-yl)methanol | HCID 7062237 | — |
Reaction Steps
2-Chloroisonicotinic acid (2.0 g; 12.7 mmol) is dissolved in 25 mL THF under anhydrous conditions and borane (1.0 M in THF; 25.4 ml; 25.4 mmol) is added drop wise via a syringe. The solution is stirred overnight at 50° C. The mixture is cooled to RT and quenched with 5 mL MeOH, concentrated under reduced pressure and purified by column chromatography on silica gel using a solvent gradient of hexanes to EtOAc. The final product is isolated as a white powder (1.1 g, 60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816082B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2a75bda1554c473fb5c7829c7d531fc4 |
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| Source note | uspto-grants-2014_08 |
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