Water → 9,9-dihexylfluorene

HRID 2252512Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2252512
[CH:1]1[C:13]2[CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH3:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].[CH2:20](Br)[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].O>O1CCCC1>[CH2:14]([C:12]1([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C:11]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[C:5]2[C:13]1=[CH:1][CH:2]=[CH:3][CH:4]=2)[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]

Komponenten

6

Edukt 4

HCID 962WaterHCID 6853FluoreneHCID 8058Hexane2×HCID 81011-Bromohexane2×

Produkt 1

HCID 51284499,9-dihexylfluoreneAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

In the stream of dry nitrogen, 5.0 g (30 mmol) of fluorene was dissolved in dry tetrahydrofuran. To this solution, 22 m l (35 mmol) of a 1.6 M hexane solution of n-butylithium was added dropwise at −78° C., and the mixture was stirred at the temperature for 1 hour. To this was then added dropwise 4.9 ml (35 mmol) of n-hexyl bromide, and the mixture was stirred at −78° C. for 1 hour, and then at room temperature for 1 hour. To the resultant, 22 ml (35 mmol) of a 1.6 M hexane solution of n-butylithium was further added dropwise at −78° C., and the mixture was stirred at the temperature for 1 hour. To this was then added dropwise 4.9 ml (35 mmol) of n-hexyl bromide, and the mixture was stirred at −78° C. for 1 hour, and then at room temperature for 1 hour. Water was added dropwise to this mixture with ice-cooling, and the resultant was then subjected to extraction with ethyl acetate. The extract was dehydrated and dried over magnesium sulfate, and the solvent was then distilled off. The residue was subjected to recrystallization from hexane to obtain 9.5 g (95%) of 9,9-dihexylfluorene.

Aufarbeitung

  1. stirringthe mixture was stirred at −78° C. for 1 hour
  2. waitat room temperature for 1 hour
  3. stirringthe mixture was stirred at the temperature for 1 hour
  4. stirringthe mixture was stirred at −78° C. for 1 hour
  5. waitat room temperature for 1 hour
  6. temperaturecooling
  7. extractionthe resultant was then subjected to extraction with ethyl acetate
  8. dry with materialdried over magnesium sulfate
  9. distillationthe solvent was then distilled off
  10. customThe residue was subjected to recrystallization from hexane

Quellen und Nachweise

ORD-Eintrag
ord-72f8b586cf574ea7bc65c7b4afb294c2
Quelldatensatz
uspto-grants-2008_01
Patentnummer
US07323225B2

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