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

HRID 2281131

Reaktionsgleichung

Reaktionsgleichung von HRID 2281131
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([CH3:12])=[CH:5]2.OO.[O-:15]S([O-])=O.[Na+].[Na+].[I-].[Na+]>C(O)(=O)C>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N+:8]([O-:15])=[CH:7][C:6]([CH3:12])=[CH:5]2

Komponenten

6

Edukt 4

HCID 784Hydrogen PeroxideHCID 5238Sodium IodideHCID 24437Sodium SulfiteHCID 157236166-Fluoro-3-methylquinoline2×

Produkt 1

HCID 867188376-Fluoro-3-methyl-quinoline 1-oxide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. temperaturebefore cooling
  2. stirringThis was stirred for 10 min
  3. custombefore partitioning between ethyl acetate and sat. NaHCO3
  4. extractionThe separated aqueous layer was extracted with ethyl acetate
  5. dry with materialthe combined organics dried over MgSO4
  6. customPurification by silica gel flash chromatography (methanol/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-1b55340e704445fba7785b65e5b6ba78
Quelldatensatz
uspto-grants-2015_09
Patentnummer
US09139538B2

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