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2,2'-Bipyridine → 6-Phenyl-2,2'-bipyridine

HRID 2117813
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2117813
[C:1]1([Li])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1CCCCC1.C(OCC)C.[N:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][N:26]=1.C(OCC)C>O>[C:1]1([C:27]2[N:26]=[C:25]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][N:19]=3)[CH:30]=[CH:29][CH:28]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 14742,2'-BipyridineHCID 3283Diethyl EtherHCID 21895417Cyclohexane diethyletherHCID 178506676HCID 178506676, Verbindung

Produkt 1

HCID 46132696-Phenyl-2,2'-bipyridineAusbeute 55,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Versuchsvorschrift

A solution of phenyllithium.cyclohexane/diethyl ether (40.9 ml, 38.4 mmol) was dropwise added to a mixture of 2,2′-bipyridine (5.0 g, 32.0 mmol) and diethyl ether (50 ml) at 5° C. while 15 minutes. This reaction mixture was stirred at room temperature for 2 hours, then the mixture was poured into water, an organic layer was separated from the mixture, furthermore an aqueous layer was extracted with dichloromethane. The organic layer was combined, and the solvent was distilled off, and the residue was diluted with acetone (50 ml), then saturated potassium permanganate acetone solution (120 ml) was added thereto, the mixture was stirred at room temperature for 1 hour. The obtained reaction mixture was filtered by Celite, the solvent of the filtrate was distilled off, and the residue was purified by silica gel column chromatography and recrystallization, thereby obtaining 4.2 g of 6-phenyl-2,2′-bipyridine as white crystal. Yield: 55.4%.

Aufarbeitung

  1. customan organic layer was separated from the mixture
  2. extractionfurthermore an aqueous layer was extracted with dichloromethane
  3. distillationthe solvent was distilled off
  4. additionthe residue was diluted with acetone (50 ml)
  5. additionsaturated potassium permanganate acetone solution (120 ml) was added
  6. stirringthe mixture was stirred at room temperature for 1 hour
  7. customThe obtained reaction mixture
  8. filtrationwas filtered by Celite
  9. distillationthe solvent of the filtrate was distilled off
  10. customthe residue was purified by silica gel column chromatography and recrystallization

Quellen und Nachweise

ORD-Eintrag
ord-7964872ef94b4462aa6cb83eb4999bbc
Quelldatensatz
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07442797B2

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