HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393975Generated: October 25, 2026
Sodium hydride → (R)-5-(Oxiran-2-ylmethoxy)quinoline
https://huagongshe.com/reaction/393975
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Glycidyl tosylate, (R)- | HCID 154187 | — |
| Reactant | Quinolin-5-ol | HCID 135441757 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-5-(Oxiran-2-ylmethoxy)quinoline | HCID 11735808 | 71.5% |
Reaction Steps
Sodium hydride (60 weight %; 1.79 g; 44.8 mmol) is washed with hexanes (3×10 mL) under an argon blanket. DMF (17 mL) is then added at ambient temperature and the stirred slurry is cooled to 5° C. A solution of 5-hydroxyquinoline (5.00 g; 34.4 mmol) in DMF (65 mL) is added dropwise over 30 minutes. The resulting mixture is allowed to warm to ambient temperature over 1 hour affording a clear, reddish-brown solution. A solution of (R)-(−)-glycidyl tosylate (10.22 g; 44.8 mmol) in DMF (50 mL) is added dropwise over 20 minutes. The resulting mixture is stirred at ambient temperature for 4 hours, quenched by the addition of saturated aqueous ammonium chloride (25 mL), poured onto water (750 mL), and extracted with ether (3×375 mL). The combined ether layers are washed with saturated aqueous sodium bicarbonate (2×375 mL), then dried over MgSO4, filtered, and concentrated in vacuo. The residue is purified via silica gel chromatography with gradient elution (33%→50% ethyl acetate in hexanes) affording the desired product (4.95 g) as a tan solid. ESMS: MH+ 202.2 (base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809093B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-6620af1544c0461a92ae36620da9a15d |
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| Source note | uspto-grants-2004_10 |
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