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Stannous Chloride → 4-Bromo-5-fluoro-1,2-benzenediamine

HRID 475210
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 475210
[Br:1][C:2]1[C:8]([F:9])=[CH:7][C:5]([NH2:6])=[C:4]([N+:10]([O-])=O)[CH:3]=1.Cl[Sn]Cl>CCO>[Br:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH2:6])=[CH:7][C:8]=1[F:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24479Stannous ChlorideHCID 219119284-Bromo-5-fluoro-2-nitroaniline

Produkt 1

HCID 199585604-Bromo-5-fluoro-1,2-benzenediamineAusbeute 43,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

To a suspension of 96 (1.57 g, 6.74 mmol) in EtOH (16 mL) was added SnCl2 (3.82 g, 20.2 mmol). The reaction mixture was heated at reflux for 14 h, cooled to RT and concentrated in vacuo. The residue was partitioned between EtOAc (100 mL) and sat'd. aq. NaHCO3 (200 mL). The resulting slurry was filtered through a pad of Celite® and the wet cake was washed with EtOAc (3×50 mL). The organic layer was washed sequentially with saturated NaHCO3, water, and brine, dried (MgSO4), filtered and concentrated in vacuo to afford 600 mg (43%) of 4-bromo-5-fluorobenzene-1,2-diamine (98) as yellow solid: MS (ESI) m/z=205 [M+1]+.

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 14 h
  3. concentrationconcentrated in vacuo
  4. customThe residue was partitioned between EtOAc (100 mL)
  5. filtrationThe resulting slurry was filtered through a pad of Celite®
  6. washthe wet cake was washed with EtOAc (3×50 mL)
  7. washThe organic layer was washed sequentially with saturated NaHCO3, water, and brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-7a9c016805e44a2d9e54cc9d32800f67
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08637537B2

Notizen zur Reaktion

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