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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795285Generated: October 31, 2026

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

https://huagongshe.com/reaction/1795285

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 difluoro-pyridin-2-yl-acetic acid ethyl ester 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 the product 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 numberUS07026324B2
Source datasetuspto-grants-2006_04
ORD IDord-914c1294352e4d2db67a4f1e09407c25
Source noteuspto-grants-2006_04