Bromine → 6-Bromo-1H-indole-3-carboxylic acid

HRID 23413

Reaktionsgleichung

Reaktionsgleichung von HRID 23413
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([OH:12])=[O:11])=[CH:2]1.[Br:13]Br>C(O)(=O)C>[Br:13][C:7]1[CH:8]=[C:9]2[C:4]([C:3]([C:10]([OH:12])=[O:11])=[CH:2][NH:1]2)=[CH:5][CH:6]=1

Komponenten

4

Edukt 2

HCID 24408BromineHCID 69867Indole-3-Carboxylic Acid

Produkt 1

HCID 152848376-Bromo-1H-indole-3-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
15 °C

Versuchsvorschrift

To a solution of indole-3-carboxylic acid (4.81 g, 30 mmole) in acetic acid (50 ml), bromine was added dropwise with stirring at 15° C. After stirring overnight at room temperature the reaction mixture was set aside without stirring for 24 hours during which time pure product crystallized from solution. The precipitate was collected and dried to afford 1.29 g pure 6-bromoindole-3-carboxylic acid. The mother liquor was poured into water (250 ml) and another crop of product was obtained (3.84 g) as a 1:1 mixture of the 6-bromo- and the 5-bromoindole-3-carboxylic acid.

Aufarbeitung

  1. stirringAfter stirring overnight at room temperature the reaction mixture
  2. stirringwithout stirring for 24 hours during which time pure product
  3. customcrystallized from solution
  4. customThe precipitate was collected
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-041984c22f354fbca34f7500f39174d9
Quelldatensatz
uspto-grants-2005_02
Patentnummer
US06852726B2

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