Imidazole → 1-(Pent-2-enyl)imidazole
Reaktionsgleichung
[CH2:1](Br)[CH:2]=[CH:3][CH2:4][CH3:5].[NH:7]1[CH:11]=[CH:10][N:9]=[CH:8]1.C(=O)(O)[O-].[Na+]>CO>[CH2:1]([N:7]1[CH:11]=[CH:10][N:9]=[CH:8]1)[CH:2]=[CH:3][CH2:4][CH3:5]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Pent-2-enyl bromide (18.5 g) was added dropwise to a stirred refluxing mixture of imidazole (10 g) and sodium bicarbonate (12.4 g) in methanol (50 ml). After addition was complete, the mixture was stirred under reflux for a further 24 hours. The mixture was filtered to remove unsoluble material and the filtrate evaporated to remove solvent. Residue taken in 2N-HCl (150 ml) and washed with ether (50 ml). The aqueous layer was basified with 10N NaOH and extracted with chloroform (3×50 ml). Combined extracts dried over anhydrous MgSO4 and chloroform removed under vacuum to leave crude product which was purified on silica gel column (EtOAc/MeOH 9:1 was used as eluent). Product fractions were collected; total weight 4.9 g. 1.0 g was distilled under vacuum; yield 1.08 g. B.p. 134° C./15 mmHg. Micro analysis: C8H12N2 requires C,70.59; H,8.82; N,20.59. Found: C,69.72, H,8.88; N,20.43.
Aufarbeitung
- temperaturerefluxing
- additionAfter addition
- temperatureunder reflux for a further 24 hours
- filtrationThe mixture was filtered
- customto remove unsoluble material
- customthe filtrate evaporated
- customto remove solvent
- washwashed with ether (50 ml)
- extractionextracted with chloroform (3×50 ml)
- dry with materialCombined extracts dried over anhydrous MgSO4 and chloroform
- customremoved under vacuum
- customto leave crude product which
- customwas purified on silica gel column (EtOAc/MeOH 9:1 was used as eluent)
- customProduct fractions were collected
- distillation1.0 g was distilled under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-f159a88e983e422e906ceecdd9ed029e
- Quelldatensatz
- uspto-grants-1981_08
- Patentnummer
- US04284641
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