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Potassium Hydroxide → 2,7-Dichloro-9-(3,7-dimethyl-octyl)-9H-carbazole

HRID 722676
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 722676
[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[NH:5][C:4]=2[CH:3]=1.[OH-].[K+].CCCCCCCC(C([NH3+])(C(CCCCCCC)=O)C(CCCCCCC)=O)=O.[Cl-].Br[CH2:49][CH2:50][CH:51]([CH3:58])[CH2:52][CH2:53][CH2:54][CH:55]([CH3:57])[CH3:56]>C(Cl)Cl>[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[N:5]([CH2:49][CH2:50][CH:51]([CH3:58])[CH2:52][CH2:53][CH2:54][CH:55]([CH3:57])[CH3:56])[C:4]=2[CH:3]=1
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Komponenten

6

Edukt 4

HCID 14797Potassium HydroxideHCID 1379141-Bromo-3,7-dimethyloctaneHCID 12070509Carbazole, 2,7-dichloro-HCID 77620884Tricaprylylmethyl ammonium chloride

Produkt 1

HCID 218856252,7-Dichloro-9-(3,7-dimethyl-octyl)-9H-carbazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

2,7-Dichlorocarbazole (synthesized according to the procedure by Leclerc et al: Morin, Jean-Francois; Leclerc, Mario; Macromolecules (2001), 34(14), 4680–4682) (10.7 g, 45.3 mmol) was added to a 50% w/w aqueous solution of potassium hydroxide (75 ml) and Aliquat-336 (0.5 ml). 1-Bromo-3,7-dimethyloctane (12.0 g, 54.3 mmol) was added dropwise and the reaction mixture was heated at 85° C. for 12 h. After cooling to room temperature, methylene chloride was added. The reaction mixture was transferred to a separation funnel and the organic layer was removed. The aqueous layer was extracted with methylene chloride (3×) and the combined organic layers were dried over magnesium sulfate. After removal of the solvent in vacuo, the crude product was purified by column chromatography (silica gel, hexane) to yield 13.5 g of the product as colorless solid.

Aufarbeitung

  1. temperatureAfter cooling to room temperature
  2. customThe reaction mixture was transferred to a separation funnel
  3. customthe organic layer was removed
  4. extractionThe aqueous layer was extracted with methylene chloride (3×)
  5. dry with materialthe combined organic layers were dried over magnesium sulfate
  6. customAfter removal of the solvent in vacuo
  7. customthe crude product was purified by column chromatography (silica gel, hexane)

Quellen und Nachweise

ORD-Eintrag
ord-0712d418553b47908225e48228690562
Quelldatensatz
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07138483B2

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