Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40630Generated: October 25, 2026

2-Methyl-5-hydroxypyridine → (S)-2-Methyl-5-oxiranylmethoxy-pyridine

https://huagongshe.com/reaction/40630

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantSodium hydrideHCID 24758—
ReactantBenzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
SolventDimethylformamideHCID 6228—
Product(S)-2-Methyl-5-oxiranylmethoxy-pyridineHCID 59686824—

Reaction Steps

6-Methyl-pyridin-3-ol (0.218 g, 2.0 mmol) was placed in a flask with DMF (10 mL) and NaH (60% dispersion in oil, 77 mg, 2.0 mmol) and stirred for 30 min. at room temperature. (S)-glycidyl 3-nitrobenzene sulfonate (0.52 g, 2.0 mmol) was then added to the reaction mixture, which was then stirred at room temperature for 14 hours. The reaction was quenched with NaHCO3 (saturated) and then extracted three times with ethyl acetate. The organic layer was dried with magnesium sulfate, filtered and the solvent was evaporated under reduced pressure to yield crude product which was purified by silica gel chromatography (60% Ethyl acetate/heptane) to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530475B2
Source datasetuspto-grants-2013_09
ORD IDord-9bf078de8aa64806aabfd30258c40a4a
Source noteuspto-grants-2013_09