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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368111Generated: October 31, 2026

Hydrogen Peroxide → 6-(Cyclopropylmethoxy)pyridin-3-ol

https://huagongshe.com/reaction/2368111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylboraneHCID 68979—
Reactant5-Bromo-2-(cyclopropylmethoxy)pyridineHCID 21914279—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6-(Cyclopropylmethoxy)pyridin-3-olHCID 57517500—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-bromo-2-(cyclopropylmethoxy)pyridine (1.88 g) in THF (15 mL) was added 1.6M n-butyllithium-hexane solution (7.25 mL) at −78° C., and the mixture was stirred at the same temperature for 20 min. Trimethylborane (1.29 mL) was added to this solution, and the mixture was stirred at −78° C. for 30 min. The reaction mixture was heated to 0° C., aqueous hydrogen peroxide (30%, 5 mL) and 8M aqueous sodium hydroxide solution (1.55 mL) were added thereto, and the mixture was stirred for 15 min. Water was added to the reaction mixture, the mixture was extracted twice with ethyl acetate, and the combined organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (855 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-c9cf9ddf13bd4a3eb8bfdb78ba40a378
Source noteuspto-grants-2014_04