Water → Triphenylene

HRID 1253380

Reaktionsgleichung

Reaktionsgleichung von HRID 1253380
[C:1]1([C:7]2[C:8]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O-])([O-])=O.[K+].[K+].O>CC(N(C)C)=O.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH:12]1[C:7]2[C:1]3[C:2](=[CH:3][CH:4]=[CH:5][CH:6]=3)[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:8]=2[CH:9]=[CH:10][CH:11]=1

Komponenten

6

Edukt 3

HCID 962WaterHCID 6766O-TerphenylHCID 11430Potassium Carbonate

Produkt 1

HCID 9170TriphenyleneAusbeute 35 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845palladium(II) acetateKatalysatorHCID 31374DimethylacetamideLösungsmittel

Versuchsvorschrift

2.87 mmol of the o-terphenyl derivative, 0.14 mmol of Pd(OAc)2 and 5.7 mmol of K2CO3 are heated in 7 ml of DMA at 135° C. for 24 hours under a nitrogen atmosphere. The reaction mixture is cooled, treated with 5 ml of water and extracted with dichloromethane. The organic phase is dried, the solvent is removed under reduced pressure and the residue is purified by means of a short silica gel column (dichloromethane). After column chromatography (dichloromethane/hexane, 2:1), the desired triphenylene derivative (IIa) is obtained in from 35 to 40% yield.

Aufarbeitung

  1. temperatureThe reaction mixture is cooled
  2. extractionextracted with dichloromethane
  3. customThe organic phase is dried
  4. customthe solvent is removed under reduced pressure
  5. customthe residue is purified by means of a short silica gel column (dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-bed0d9afd4144f1387089f43035b718c
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08455112B2

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