2-Phenylbenzimidazole → 1-Methyl-2-phenylbenzimidazole

HRID 49692

Reaktionsgleichung

Reaktionsgleichung von HRID 49692
[C:1]1([C:7]2[NH:8][C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:16]1CCN2C(=NCCC2)CC1>>[CH3:16][N:11]1[C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[N:8]=[C:7]1[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

3

Edukt 2

HCID 128552-PhenylbenzimidazoleHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

Produkt 1

HCID 758071-Methyl-2-phenylbenzimidazole

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a mixture of 2-phenylbenzimidazole (1.02 g, 5.25 mmol) in DMC (10 mL), DBU (0.80 g, 5.25 mmol) was added and the resulting mixture was heated to reflux (90° C.) for 6 hours. The solvent was evaporated under vacuum and the resulting oil was dissolved in methylene chloride (2 mL) and filtered through silica gel (2:1 EtOA/hexane). The solvent was evaporated under vacuum to afford 1-methyl-2-phenylbenzimidazole as a solid. The yield of 1-methyl-2-phenylbenzimiazole as determined by HPLC analysis was 98%.

Aufarbeitung

  1. additionwas added
  2. temperaturethe resulting mixture was heated
  3. customThe solvent was evaporated under vacuum
  4. dissolutionthe resulting oil was dissolved in methylene chloride (2 mL)
  5. filtrationfiltered through silica gel (2:1 EtOA/hexane)
  6. customThe solvent was evaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-ff7dc106ad254b359a888c4714010314
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06706929B2

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