HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843355Generated: October 30, 2026
6-Hydroxyquinoline → HCID 59885584, compound
https://huagongshe.com/reaction/843355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Hydroxyquinoline | HCID 11374 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Glycidyl tosylate, (R)- | HCID 154187 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59885584 | HCID 59885584 | 67.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376514B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-56958230c0714d73b6ff31178c7377ff |
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| Source note | uspto-grants-2002_04 |
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