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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657739Generated: October 30, 2026

Sodium Azide → (S)-2-azido-2-(6-methoxypyridin-3-yl)ethanol

https://huagongshe.com/reaction/657739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantLithium perchlorateHCID 23665649—
Reactant2-methoxy-5-[(2R)-oxiran-2-yl]pyridineHCID 58103576—
SolventAcetonitrileHCID 6342—
Product(S)-2-azido-2-(6-methoxypyridin-3-yl)ethanolHCID 5810359369%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of (R)-2-methoxy-5-(oxiran-2-yl)pyridine (1.02 g, 6.75 mmol) in acetonitrile (100 mL) were added sodium azide (1.8 g, 27 mmol) and lithium perchlorate (11 g, 0.10 mol) and the mixture was stirred at 60° C. for 4 h. TLC indicated completion of the reaction. After cooling, the mixture was filtered through Celite and the filtrate was concentrated. The residue was treated with water and extracted with EtOAc (3×50 mL). The combined organic layers were washed with aq. NaHCO3 and brine, dried (Na2SO4), and concentrated. The residue was purified by silica gel column (0-50% EtOAc/hexane) to yield a light yellow oil (0.9 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076345B2
Source datasetuspto-grants-2011_12
ORD IDord-1d4e35a528ab499cb3969b78fd59587c
Source noteuspto-grants-2011_12