Chlorotrimethylsilane → HCID 23448979, Verbindung

HRID 989862Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 989862
C([Li])CCC.CCCCCC.[CH3:12][S:13][C:14]1[N:15]=[CH:16][N:17]2[CH:21]=[CH:20][S:19][C:18]=12.[CH3:22][Si:23](Cl)([CH3:25])[CH3:24].[Cl-].[NH4+]>C1COCC1>[CH3:12][S:13][C:14]1[N:15]=[CH:16][N:17]2[CH:21]=[C:20]([Si:23]([CH3:25])([CH3:24])[CH3:22])[S:19][C:18]=12

Komponenten

6

Reaktionsbedingungen

Temperatur
-30 °C

Versuchsvorschrift

A 1.59 N n-butyllithium/n-hexane solution (9.91 ml) was added dropwise in an argon atmosphere at −50° C. to a solution of 2.55 g of 7-methylthioimidazo[5,1-b]thiazole in 100 ml of THF. The mixture was stirred at the same temperature for 25 min. Trimethylsilyl chloride (2.08 ml) was added thereto, and the mixture was stirred for 30 min. The temperature of the system was raised to −30° C. A 1.59 N n-butyllithium/n-hexane solution (5.72 ml) was added dropwise thereto, and the mixture was stirred at the same temperature for 30 min. An aqueous ammonium chloride solution was added to the reaction solution. The mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and then filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:2) to give 2.58 g of 7-methylthio-2-trimethylsilylimidazo[5,1-b]-thiazole.

Aufarbeitung

  1. stirringthe mixture was stirred for 30 min
  2. stirringthe mixture was stirred at the same temperature for 30 min
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialThe extract was dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. customThe solvent was removed by distillation under the reduced pressure
  7. customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:2)

Quellen und Nachweise

ORD-Eintrag
ord-43263a4ab88044daa5cf300af4996335
Quelldatensatz
uspto-grants-2002_10
Patentnummer
US06458780B1

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