HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717868Generated: November 2, 2026
Sodium borohydride → 2-Chloro-6-(trifluoromethyl)-4-pyridinemethanol
https://huagongshe.com/reaction/717868
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2-chloro-6-(trifluoromethyl)isonicotinate | HCID 71433010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Chloro-6-(trifluoromethyl)-4-pyridinemethanol | HCID 72212583 | — |
Reaction Steps
Sodium tetrahydroborate (74 mg, 2.0 mmol) was added to a solution of ethyl 2-chloro-6-(trifluoromethyl)isonicotinate (0.50 g, 2.0 mmol, Anichem) in ethanol (17 mL) at 0° C. The mixture was stirred at 0° C. for one hour, then was allowed to warm to room temperature and stir for 2 hours. The mixture was recooled in an ice bath and was quenched by the dropwise addition of 4.0 mL 1N HCl. The pH was then adjusted to 7 by the addition of saturated sodium bicarbonate solution. The reaction was further diluted with water, and then was extracted with EtOAc. The extract was washed with brine, dried over sodium sulfate, filtered and concentrated. Flash chromatography on silica gel, eluting with a gradient from 0-40% EtOAc in Hexanes afforded product as an oil (0.33 g, 79%). 1H NMR (300 MHz, CDCl3) δ 7.61 (s, 1H), 7.56 (s, 1H), 4.84 (d, J=5.2 Hz, 2H), 2.20 (t, J=5.6 Hz, 1H); LCMS (M+H)+: 212.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193733B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-7f64fe4383f744adb29a2e29f3172a12 |
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| Source note | uspto-grants-2015_11 |
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