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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338553Generated: October 26, 2026

Potassium Hydroxide → (3S)-1-(6-methoxypyridin-2-yl)pyrrolidin-3-ol

https://huagongshe.com/reaction/338553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloro-6-methoxypyridineHCID 87009—
Reactant(3S)-pyrrolidin-3-olHCID 2733874—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystBippyPhosHCID 11547931—
SolventMeOH tetrahydrofuranHCID 21899815—
Product(3S)-1-(6-methoxypyridin-2-yl)pyrrolidin-3-olHCID 86698868226.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-chloro-6-methoxypyridine (1.966 g, 3.750 mmol) and commercially available (3S)-pyrrolidin-3-ol (1.437 g, 16.50 mmol) in tetrahydrofuran/methanol (137 mL/6.7 mL), was added Pd2(dba)3 (62.2 mg, 0.0688 mmol), BippyPhos (139.2 mg, 0.2750 mmol) and potassium hydroxide (1.16 g, 20.6 mmol, 88% pellets). The reaction was then was purged with nitrogen for 2 minutes and stirred at 70° C. for 18 hours. The reaction was filtered, quenched with saturated ammonium chloride solution, adjusted to pH=7˜8 with 1N hydrochloric acid and extracted with dichloromethane (100 mL*2) and ethyl acetate (100 mL*3). The combined organic phase was washed with saturated brine, dried over sodium sulfate and evaporated in vacuo. The residue was then purified by silica gel chromatography with ethyl acetate/petroleum ether, 0-25% to give the title compound (1.65 g, 62%) as a yellow gum that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-72e6bcacd29247ffb74c40060173fe7c
Source noteuspto-grants-2014_11