Bromoform → 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile

HRID 1920252

Reaktionsgleichung

Reaktionsgleichung von HRID 1920252
N(OC(C)(C)C)=O.N[C:9]1[N:13]([CH2:14][CH:15]([CH3:17])[CH3:16])[C:12]([CH2:18][CH2:19][CH2:20][CH3:21])=[N:11][C:10]=1[C:22]#[N:23].C(Br)(Br)[Br:25]>>[Br:25][C:9]1[N:13]([CH2:14][CH:15]([CH3:17])[CH3:16])[C:12]([CH2:18][CH2:19][CH2:20][CH3:21])=[N:11][C:10]=1[C:22]#[N:23]

Komponenten

4

Edukt 3

HCID 5558BromoformHCID 10906Tert-Butyl nitriteHCID 58500139HCID 58500139, Verbindung

Produkt 1

HCID 585001335-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrileAusbeute 39 %

Versuchsvorschrift

tert-Butyl nitrite (6.2 g, 0.060 mol) was added over a period of five minutes to solution of 5-amino-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile (6.60 g, 30.0 mmol) in bromoform (50 mL). After about ten minutes, an exotherm occurred, and the reaction was poured into ice water. The reaction temperature peaked at 55° C. The reaction was stirred at room temperature for 45 minutes and then concentrated under reduced pressure while heating at about 55° C. The crude product (20 g) was purified by column chromatography on silica gel (eluting sequentially with dichloromethane and 5% ethyl acetate in dichloromethane) to provide 3.37 g (39%) of 5-bromo-2-butyl-1-(2-methylpropyl)-1H-imidazole-4-carbonitrile as an orange oil.

Aufarbeitung

  1. waitAfter about ten minutes
  2. custompeaked at 55° C
  3. concentrationconcentrated under reduced pressure
  4. temperaturewhile heating at about 55° C
  5. customThe crude product (20 g) was purified by column chromatography on silica gel (
  6. washeluting sequentially with dichloromethane and 5% ethyl acetate in dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-1e5eb36df7484d1b81be63192b09d8f7
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08168802B2

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