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Hydrochloric Acid → 3-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

HRID 414378
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 414378
[Br:1][C:2]1[C:8]([F:9])=[C:7]([F:10])[CH:6]=[C:5]([N+:11]([O-:13])=[O:12])[C:3]=1N.C(ON=O)(C)(C)C.[ClH:21]>C(#N)C>[Br:1][C:2]1[C:3]([Cl:21])=[C:5]([N+:11]([O-:13])=[O:12])[CH:6]=[C:7]([F:10])[C:8]=1[F:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 140717912-Bromo-3,4-difluoro-6-nitroaniline

Produkt 1

HCID 140717923-Bromo-2-chloro-4,5-difluoro-1-nitrobenzene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To a mixture of anhydrous cupric chloride (3.1 g) and 2 -bromo-3,4-difluoro-6-nitroaniline (4.6 g) in anhydrous acetonitrile (30 ml) was added t-butylnitrite (2.8 g) dropwise at 51° to 56° C. during 5 minutes. After stirring for 8 minutes at the same temperature, the reaction mixture was poured into chilled 10% diluted hydrochloric acid (30 ml) and extracted with benzene. The organic layer was washed with diluted hydrochloric acid and with water successively, dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified by silica gel chromatography eluting with dichloromethane-n-hexane (1:5) to give the title compound (4.0 g).

Aufarbeitung

  1. additionthe reaction mixture was poured
  2. extractionextracted with benzene
  3. washThe organic layer was washed with diluted hydrochloric acid and with water successively
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe resulting residue was purified by silica gel chromatography
  7. washeluting with dichloromethane-n-hexane (1:5)

Quellen und Nachweise

ORD-Eintrag
ord-219fa7f0beb546739c344bcd9c741062
Quelldatensatz
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04791225

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