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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720926Generated: October 31, 2026

Sodium hydride → HCID 59885608, compound

https://huagongshe.com/reaction/720926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantGlycidyl tosylate, (R)-HCID 154187—
ReactantQuinolin-5-olHCID 135441757—
SolventDimethylformamideHCID 6228—
ProductHCID 59885608HCID 5988560816%

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 10 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 10 minutes. The resulting mixture is stirred at ambient temperature for 20.5 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 (50%→60% acetone in hexanes) affording the desired product (1.11 g) as a tan solid. ESMS:MH+ 202.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135483B2
Source datasetuspto-grants-2006_11
ORD IDord-fbfca954ef6241088ff732db58edbc49
Source noteuspto-grants-2006_11