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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2281131Erstellt: 27. Oktober 2026

Hydrogen Peroxide → 6-Fluoro-3-methyl-quinoline 1-oxide

https://huagongshe.com/reaction/2281131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktSodium IodideHCID 5238—
EduktSodium SulfiteHCID 24437—
Edukt6-Fluoro-3-methylquinolineHCID 15723616—
LösungsmittelAcetic AcidHCID 176—
Produkt6-Fluoro-3-methyl-quinoline 1-oxideHCID 86718837—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

6-Fluoro-3-methyl-quinoline (Intermediate 28) (48.0 mg, 0.298 mmol) was dissolved in acetic acid (1 mL) and 30% aqueous H2O2 (0.040 mL, 0.396 mmol) was added. This was stirred at 80° C. for 16 h before cooling. A few mLs of a 10% aq. solution of Na2SO3 was added followed by a spatula tip of sodium iodide. This was stirred for 10 min before partitioning between ethyl acetate and sat. NaHCO3. The separated aqueous layer was extracted with ethyl acetate and the combined organics dried over MgSO4. Purification by silica gel flash chromatography (methanol/ethyl acetate) gave 6-fluoro-3-methyl-quinoline 1-oxide (29.4 mg) as a white solid. 1H NMR (400 MHz, CDCl3) δ 8.72 (dd, J=9.4, 5.3 Hz, 1 H) 8.38 (s, 1 H) 7.36-7.50 (m, 3 H) 2.46 (s, 3 H); MS (M+1): 178.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09139538B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-1b55340e704445fba7785b65e5b6ba78
Quellennotizuspto-grants-2015_09