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N-bromobutanimide → 5-Bromo-4,6-difluoroindoline

HRID 338228
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 338228
[F:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][NH:6]2.[Br:12]N1C(=O)CCC1=O>C(#N)C>[Br:12][C:10]1[C:2]([F:1])=[C:3]2[C:7](=[CH:8][C:9]=1[F:11])[NH:6][CH2:5][CH2:4]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 67184N-bromobutanimideHCID 162444494,6-Difluoro-2,3-dihydro-1H-indole

Produkt 1

HCID 838958425-Bromo-4,6-difluoroindolineAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To a solution of 4,6-difluoroindoline (4.6 g, 29.8 mmol) in acetonitrile (50 mL) was added a solution of N-bromosuccinimide (3.68 g, 20.6 mmol) acetonitrile (30 mL) at 0° C. dropwise. The reaction was stirred for 30 minutes and quenched with saturated aqueous sodium bicarbonate solution and diluted with ethyl acetate. The layers were separated and the organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (0-60% ethyl acetate in petroleum ether) to give the title compound (4.0 g, 58% yield) as colorless oil

Aufarbeitung

  1. customquenched with saturated aqueous sodium bicarbonate solution
  2. additiondiluted with ethyl acetate
  3. customThe layers were separated
  4. dry with materialthe organic phases were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography (0-60% ethyl acetate in petroleum ether)

Quellen und Nachweise

ORD-Eintrag
ord-3c79293afe6a4d389402c07a59cecca4
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08889730B2

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