HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397471Generated: October 25, 2026
Sodium borohydride → 2,2-Difluoro-2-(pyridin-2-YL)ethanol
https://huagongshe.com/reaction/397471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl difluoro(pyridin-2-yl)acetate | HCID 10631894 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2-Difluoro-2-(pyridin-2-YL)ethanol | HCID 9942216 | — |
Reaction Steps
To a stirred solution of 19.5 g (97 mmol) of ethyl difluoro-2-pyridylacetate I-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 I-1-3 as a beige crystalline solid: 1H NMR (CDCl3) δ3.6 (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610701B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-dc684ae29fcd44b7a46021a98d05aefa |
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| Source note | uspto-grants-2003_08 |
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