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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281898Generated: October 25, 2026

Sodium borohydride → 2,2-Difluoro-2-(pyridin-2-YL)ethanol

https://huagongshe.com/reaction/1281898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl difluoro(pyridin-2-yl)acetateHCID 10631894—
SolventEthanolHCID 702—
Product2,2-Difluoro-2-(pyridin-2-YL)ethanolHCID 9942216—

Reaction Steps

To a stirred solution of 19.5 g (97 mmol) of ethyl difluoro-2-pyridylacetate 1-2 in 200 mL of absolute ethanol at 0° C. was added 4.42 g (116 mmol) of sodium borohydride in small portions. After 30 min, the reaction was quenched by the addition of 50 mL of sat. NH4Cl. The reaction mixture was concentrated at reduced pressure and the residue partitioned between 500 mL of ethyl acetate and sat. NaHCO3. The organic layer was washed with water, brine, and dried over Na2SO4 and concentrated at reduced pressure to give a brown oil that was purified on SiO2 (10×17 cm) using 1:1 EtOAc-hexane. After re-chromatographing the mixed fractions, all clean fractions were combined and concentrated at reduced pressure, giving 1-3 as a beige crystalline solid: 1H NMR (CDCl3) δ 3.6 (t, 1H), 4.17-4.3 (m, 2H), 7.4-7.45 (m, 1H), 7.73 (d, 1H), 7.84-7.91 (m, 1H), 8.61 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455532B1
Source datasetuspto-grants-2002_09
ORD IDord-2e43b58940aa45718d07ca4fb21218ad
Source noteuspto-grants-2002_09