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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Lithium perchlorate | HCID 23665649 | — |
| Reactant | 2-methoxy-5-[(2R)-oxiran-2-yl]pyridine | HCID 58103576 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-2-azido-2-(6-methoxypyridin-3-yl)ethanol | HCID 58103593 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076345B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-1d4e35a528ab499cb3969b78fd59587c |
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| Source note | uspto-grants-2011_12 |
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