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2-Chloromethyl 2-(trimethylsilyl)ethyl ether → 5-Methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole

HRID 448008
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 448008
[CH3:1][C:2]1[N:3]=[CH:4][N:5](C(=O)C)[CH:6]=1.[CH3:10][Si:11]([CH2:14][CH2:15][O:16][CH2:17]Cl)([CH3:13])[CH3:12]>C(#N)C>[CH3:1][C:2]1[N:3]([CH2:17][O:16][CH2:15][CH2:14][Si:11]([CH3:13])([CH3:12])[CH3:10])[CH:4]=[N:5][CH:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 109534921-Acetyl-4-methylimidazole

Produkt 1

HCID 597712705-Methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazoleAusbeute 61,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a solution of 4-methylimidazole (2.70 g, 33.0 mmol) in 10 mL of acetonitrile at 0° C. was added triethylamine (NEt3) (4.00 g, 39.6 mmol) and acetyl chloride (2.80 g, 36.3 mmol). The mixture was allowed to attain RT then filtered to remove the ppt and the filtrate was concentrated to give 1-(4-methyl-imidazol-1-yl)-ethanone, which was used without further purification in the next step. To a solution of 1-(4-methyl-imidazol-1-yl)-ethanone (4.10 g, 33.0 mmol) in 15 mL acetonitrile was added SEM-Cl (5.80 g, 35.0 mmol) and the solution was stirred at 25° C. for 10 h. The solvents were removed by evaporation and to the residue was added 100 mL of 2.5 M NaOH and the mixture was stirred at 25° C. for 1 h. The reaction mixture was then extracted with ether (3×100 mL), dried over Na2SO4 and concentrated. The title compound was purified by chromatography on silica gel eluting with 75% EtOAc/hexanes to give 4.30 g (61%) of a colorless oil: Mass spectrum (ESI, m/z): Calcd. for C10H20N2O4Si, 213.1 (M+H), found 213.1.

Aufarbeitung

  1. customwas used without further purification in the next step
  2. customThe solvents were removed by evaporation and to the residue
  3. additionwas added 100 mL of 2.5 M NaOH
  4. stirringthe mixture was stirred at 25° C. for 1 h
  5. extractionThe reaction mixture was then extracted with ether (3×100 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe title compound was purified by chromatography on silica gel eluting with 75% EtOAc/hexanes

Quellen und Nachweise

ORD-Eintrag
ord-d669f9d815104fda85a8499ee5ada0a5
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08481564B2

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