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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantGlycidyl tosylate, (R)-HCID 154187—
ReactantQuinolin-5-olHCID 135441757—
SolventDimethylformamideHCID 6228—
Product(R)-5-(Oxiran-2-ylmethoxy)quinolineHCID 1173580871.5%

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809093B2
Source datasetuspto-grants-2004_10
ORD IDord-6620af1544c0461a92ae36620da9a15d
Source noteuspto-grants-2004_10