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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386802Generated: October 31, 2026

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

https://huagongshe.com/reaction/1386802

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 EXAMPLE 202, 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 iceli-PrOH 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. NH4Cl (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. NaCl (100 mL) and extracted with EtOAc (4×75 mL). The combined organic layers were dried (Na2SO4), 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 numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-8326c5519a274a99bbce72723119fc17
Source noteuspto-grants-2001_07