Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862699Generated: November 2, 2026

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

https://huagongshe.com/reaction/1862699

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. A part. 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 numberUS06538002B1
Source datasetuspto-grants-2003_03
ORD IDord-f5d355be920e42d8bdcd5d7fc8ae8ce3
Source noteuspto-grants-2003_03