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5,6-Dimethyl-2-trifluoromethylbenzimidazole → HCID 15376227, Verbindung

HRID 2256398
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2256398
[CH3:1][C:2]1[C:14]([CH3:15])=[CH:13][C:5]2[NH:6][C:7]([C:9]([F:12])([F:11])[F:10])=[N:8][C:4]=2[CH:3]=1.[H-].[Na+].[CH3:18][O:19][C:20](=[O:29])[C:21]1[CH:26]=[CH:25][C:24]([CH2:27]Br)=[CH:23][CH:22]=1>CN(C=O)C>[CH3:18][O:19][C:20](=[O:29])[C:21]1[CH:26]=[CH:25][C:24]([CH2:27][N:8]2[C:4]3[CH:3]=[C:2]([CH3:1])[C:14]([CH3:15])=[CH:13][C:5]=3[N:6]=[C:7]2[C:9]([F:12])([F:10])[F:11])=[CH:23][CH:22]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 157255,6-Dimethyl-2-trifluoromethylbenzimidazoleHCID 24758Sodium hydrideHCID 256687Methyl 4-(bromomethyl)benzoate

Produkt 1

HCID 15376227HCID 15376227, VerbindungAusbeute 23,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

5,6-Dimethyl-2-trifluoromethyl-1H-benzoimidazole (2.14 g, 0.01 mol) was dissolved in DMF (50 mL). Sodium hydride (60% dispersion in oil, 0.48 g, 0.012 mol) was added and the reaction mixture was stirred at ambient temperature for 0.5 hour under an atmosphere of nitrogen. 4-Bromomethyl benzoic acid methyl ester (2.29 g, 0.01 mol) was then added. The mixture was stirred at 80° C. for 18 hours. Most of the solvent was evaporated. The residue was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous sodium sulfate then evaporated. The residue was crystallized from ethyl acetate/hexane twice to afford pure title compound (0.85 g, 23.5% yield) as a white solid, m.p. 150°-152° C. Anal. Calcd. for C19H17F3N2O2 : C, 62.98; H, 4.73; N, 7.73. Found: C, 62.96; H, 4.73; N, 7.56. Mass spectrum (+FAB; [M+H]+) 363. 1H-NMR (DMSO-d6 ; 400 MHz) δ 7.90 (d, 1H), 7.63 (s, 1H), 7.45 (s, 1H), 7.15 (d, 2H), 5.74 (s, 2H), 3.81 (s, 3H), 2.33 (s, 3H), and 2.30 ppm (s, 3H).

Aufarbeitung

  1. stirringThe mixture was stirred at 80° C. for 18 hours
  2. customMost of the solvent was evaporated
  3. additionThe residue was diluted with water
  4. extractionextracted with ethyl acetate
  5. washThe organic phase was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customthen evaporated
  8. customThe residue was crystallized from ethyl acetate/hexane twice

Quellen und Nachweise

ORD-Eintrag
ord-5ae0fb11f64a4f349fa9a36f0daa11e7
Quelldatensatz
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05654436

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