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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-chloro-6-(trifluoromethyl)isonicotinateHCID 71433010—
SolventEthanolHCID 702—
Product2-Chloro-6-(trifluoromethyl)-4-pyridinemethanolHCID 72212583—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193733B2
Source datasetuspto-grants-2015_11
ORD IDord-7f64fe4383f744adb29a2e29f3172a12
Source noteuspto-grants-2015_11