1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 178440796, Verbindung

HRID 1067667Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1067667
[Br-].[C:2]1([CH2:8][CH2:9][CH2:10][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:37]2[CH:41]=[C:40](C=O)[N:39]=[CH:38]2)C=CC=CC=1.[K].[C:57]([O-])(C)(C)C>C1COCC1>[NH:37]1[CH:41]=[C:40]([CH:9]([CH2:8][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:10]=[CH2:57])[N:39]=[CH:38]1

Komponenten

6

Versuchsvorschrift

10 mmol of 3-phenylpropyltriphenylphosphonium bromide, 10 mmol of (1-triphenylmethyl-1H-imidazol-4-yl)methanal (J. L. Kelley, C. A. Miller, E. W. Mc Lean, J. Med. Chem. 1977, 20, 721) and 12 mmol of potassium of t-butanolate are stirred for 24 hours in 50 ml THF. The solvent is evaporated off under reduced pressure, hydrolysed with water and extracted using chloroform. The concentrated organic extract is heated from reflux in 30 ml 2N HCl and 30 ml of acetone for 1 hour. The solvent is evaporated off under reduced pressure and triphenylmethanol is extracted using diethyl ether. The aqueous phase is alkalized using ammonia and the crude product is extracted using diethyl ether. The aqueous phase is alkalized using diethyl ether and crystallized as hydrogen maleate from diethyl ether and ethanol.

Aufarbeitung

  1. customThe solvent is evaporated off under reduced pressure, hydrolysed with water
  2. extractionextracted
  3. extractionThe concentrated organic extract
  4. temperatureis heated
  5. temperaturefrom reflux in 30 ml 2N HCl
  6. customThe solvent is evaporated off under reduced pressure and triphenylmethanol
  7. extractionis extracted
  8. extractionthe crude product is extracted
  9. customcrystallized as hydrogen maleate from diethyl ether and ethanol

Quellen und Nachweise

ORD-Eintrag
ord-a4c6ae19dac64578b2008e550852aea2
Quelldatensatz
uspto-grants-2001_06
Patentnummer
US06248765B1

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