Reaktion #2161291

ord-b6222423c6fe42c1ac54d1d9d01966a5

Reaktionsgleichung

CC(O)c1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
1-(1-trityl-1H-imidazol-4-yl)ethanol
CC(=O)c1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
title compound
Ausbeute 100.4%
CC(=O)c1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
1-(1-trityl-1H-imidazol-4-yl)ethanone
Ausbeute 100.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was refluxed for 2 hours
  2. 2
    Sonstigewas consumed completely
  3. 3
    Filtrationthe mixture was filtered
  4. 4
    WaschenThe filter cake was washed with dry CH2Cl2 (5×50 mL)
  5. 5
    Sonstigethe filtrate was evaporated

Vorschrift

To a solution of 1-(1-trityl-1H-imidazol-4-yl)ethanol (4.0 g, 11.3 mmol) in anhydrous 1,4-dioxane (150 mL) was added activated MnO2 (2.5 g, 28.2 mmol) at 0° C. The mixture was refluxed for 2 hours. TLC (EtOAc/Petroleum ether 1:2) showed the starting material was consumed completely, and the mixture was filtered. The filter cake was washed with dry CH2Cl2 (5×50 mL) and the filtrate was evaporated to afford the title compound (4.0 g, 100%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07919488B2uspto-grants-2011_04