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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303660Generated: November 2, 2026

Sodium borohydride → 2,2-Difluoro-2-(2-pyridyl)-1-methoxyethanol

https://huagongshe.com/reaction/2303660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl difluoro(pyridin-2-yl)acetateHCID 10631894—
SolventMethanolHCID 887—
Product2,2-Difluoro-2-(2-pyridyl)-1-methoxyethanolHCID 18187512108.5%

Reaction Steps

Ethyl difluoro(2-pyridyl)acetate (1.00 g, 4.97 mmol, from Procedure 35, Step B) was dissolved in CH3OH (15 mL) in a 3-neck round bottom flask fitted with a mechanical stirrer, and the resulting solution was cooled in a dry ice/isopropanol bath. Sodium borohydride (114 mg, 3.0 mmol) was added in 2 portions 15 min. apart. After an additional 55 min., the cold reaction was quenched by the addition of saturated aq. ammonium chloride (6.5 mL) over 12 min. After 10 min., the cooling bath was removed and the mixture was stirred for 35 min. before being diluted with saturated aq. brine (100 mL) and extracted with ethyl acetate (4×75 mL). The combined organic layers were dried (sodium sulfate), decanted, and evaporated to give 1.02 g of crude 2,2-difluoro-2-(2-pyridyl)-1-methoxyethanol as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-eb171e93c8194a4bb91a5565dd8dd249
Source noteuspto-grants-2002_08