Sodium Hydroxide → 7-Bromo-3-chloro-4-methyl-1H-indole

HRID 1173095Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1173095
[Cl:1]N1C(=O)CCC1=O.[Br:9][C:10]1[CH:11]=[CH:12][C:13]([CH3:19])=[C:14]2[C:18]=1[NH:17][CH:16]=[CH:15]2.BrC1C=CC(C)=CC=1[N+]([O-])=O.[OH-].[Na+]>C(#N)C>[Br:9][C:10]1[CH:11]=[CH:12][C:13]([CH3:19])=[C:14]2[C:18]=1[NH:17][CH:16]=[C:15]2[Cl:1]

Komponenten

6

Edukt 4

HCID 14798Sodium HydroxideHCID 31398ChlorosuccinimideHCID 792244-Bromo-3-nitrotolueneHCID 187528627-bromo-4-methyl-1H-indole

Produkt 1

HCID 223592387-Bromo-3-chloro-4-methyl-1H-indoleAusbeute 99,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

4.0 g (30.0 mmol) of N-chlorosuccinimide was added to an acetonitrile solution (250 ml) containing 5.8 g (27.6 mmol) of 7-bromo-4-methyl-1H-indole synthesized from 2-bromo-5-methylnitrobenzene in the same manner as in Production Example 1a, followed by stirring at room temperature overnight. 50 ml of a 1N aqueous sodium hydroxide was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and concentrated. Then, the residue was purified by silica gel column chromatography, to give 6.7 g of the title compound.

Aufarbeitung

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with water
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated
  5. customThen, the residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-d235fdf7bdbd4931b5e69360ffa74e6f
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07834049B2

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