HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426241Generated: October 30, 2026
Hydrochloric Acid → (2-Chloropyridin-4-yl)methanol
https://huagongshe.com/reaction/426241
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloroisonicotinic acid | HCID 236985 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Chloropyridin-4-yl)methanol | HCID 7062237 | 5,990.1% |
Reaction Steps
To a stirred solution of 2-chloroisonicotinic acid (3.15 g, 20 mmol) in anhydrous THF (40 ml) cooled in an ice bath, was added borane-methyl sulfide complex (6 mL, 60 mmol). After 1 hr, the mixture was stirred for 48 hr at room temperature. The mixture was cooled in an ice bath and conc. HCl (30 ml) was added and stirred for 30 min. The mixture was then basified by addition of 50% aqueous NaOH (30 ml). The product was extracted with dichloromethane, dried with anhydrous potassium carbonate, filtered, and evaporated in vacuo. The crude product was purified by silica gel column chromatography (eluent, ether:hexane (5:1)) to afford 172 g (60%) of 2-chloro-4-pyridinemethanol as a white solid. m.p. 77-79° C.; 1H NMR (200 MHz, CDCl3) δ 2.97 (1H, br. s), 4.74 (2H, s), 7.20 (1H, d, J=5.7 Hz), 7.36 (1H, s), 8.28 (1H, d, J=5.7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106064B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-a1cefcc5119840f29ddf09ec610d3f14 |
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| Source note | uspto-grants-2012_01 |
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