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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843355Generated: October 30, 2026

6-Hydroxyquinoline → HCID 59885584, compound

https://huagongshe.com/reaction/843355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-HydroxyquinolineHCID 11374—
ReactantSodium hydrideHCID 24758—
ReactantGlycidyl tosylate, (R)-HCID 154187—
SolventDimethylformamideHCID 6228—
ProductHCID 59885584HCID 5988558467.7%

Reaction Conditions

Temperature5 °C

Reaction Steps

Sodium hydride (60 weight %; 0.36 g; 9.0 mmol) is washed with hexanes (3×5 mL) under an argon blanket. DMF (3 mL) is then added at ambient temperature and the stirred slurry is cooled to 5° C. A solution of 6-hydroxyquinoline (1.00 g; 6.9 mmol) in DMF (13 mL) is added dropwise over 10 minutes. The resulting mixture is allowed to warm to ambient temperature over 30 minutes affording a clear, reddish-brown solution. A solution of (R)-(−)-glycidyl tosylate (2.04 g; 9.0 mmol) in DMF (10 mL) is added dropwise over 10 minutes. The resulting mixture is stirred at ambient temperature for 13 hours, quenched by the addition of saturated aqueous ammonium chloride (5 mL), poured onto water (150 mL), and extracted with ether (3×75 mL). The combined ether layers are washed with saturated aqueous sodium bicarbonate (2×75 mL), then dried over MgSO4, filtered, and concentrated in vacuo. The residue is purified via silica gel chromatography with gradient elution (40%→70% ethyl acetate in hexanes) affording the desired product (0.94 g) as an oil. CIMS: MH+ 202.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376514B1
Source datasetuspto-grants-2002_04
ORD IDord-56958230c0714d73b6ff31178c7377ff
Source noteuspto-grants-2002_04