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Hydrogen Peroxide → 3-(5-Bromo-2-fluorophenyl)pyridine-1-oxide

HRID 2184003
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2184003
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:14])=[C:6]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)[CH:7]=1.C(OO)(=[O:17])C.OO>C(O)(=O)C.O1CCCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:14])=[C:6]([C:8]2[CH:9]=[N+:10]([O-:17])[CH:11]=[CH:12][CH:13]=2)[CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 784Hydrogen PeroxideHCID 6585Peracetic AcidHCID 115433553-(5-Bromo-2-fluorophenyl)pyridine

Produkt 1

HCID 224735943-(5-Bromo-2-fluorophenyl)pyridine-1-oxideAusbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittel
HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A mixture of 3-(5-bromo-2-fluorophenyl)pyridine (2.52 g, 10.0 mmol) and peracetic acid (3.37 ml of a 36-40 wt % solution in acetic acid) in tetrahydrofuran (40 ml) was stirred at ambient temperature for 1 h and then heated at 50° C. for 2 h. Hydrogen peroxide (35 wt % solution in water, 1 ml) was added and the mixture heated at 50° C. for a further hour. The solvent was removed in vacuo and the residue diluted with water and layered with ethyl acetate. Solid sodium hydrogencarbonate was added to pH 8. The layers were separated and the organic layer washed with water, brine, dried over anhydrous magnesium sulfate, filtered and pre-adsorbed onto silica. Purification by flash column chromatography on silica gel eluting with dichloromethane (containing 1% ammonia) on a gradient of methanol (2-5%) gave 3-(5-bromo-2-fluorophenyl)pyridine-1-oxide as a white solid (2.00 g, 75%): δH (400 MHz, CDCl3) 7.09-7.14 (1H, m), 7.35-7.43 (2H, m), 7.52-7.57 (2H, m), 8.22-8.25 (1H, m), 8.42 (1H, t, J 1).

Aufarbeitung

  1. temperatureheated at 50° C. for 2 h
  2. temperaturethe mixture heated at 50° C. for a further hour
  3. customThe solvent was removed in vacuo
  4. additionthe residue diluted with water
  5. additionSolid sodium hydrogencarbonate was added to pH 8
  6. customThe layers were separated
  7. washthe organic layer washed with water, brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered and pre-adsorbed onto silica
  10. customPurification by flash column chromatography on silica gel eluting with dichloromethane (containing 1% ammonia) on a gradient of methanol (2-5%)

Quellen und Nachweise

ORD-Eintrag
ord-d0d063c6c1d04c39834c831292ec4114
Quelldatensatz
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06900215B2

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