Reaktion #159488

ord-c009799bd0b448ae8de99f5d4e0eb69a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITthe mixture is left
  2. 2
    workup.WAITto stand overnight
  3. 3
    EinengenThe reaction mixture is concentrated in vacuo
  4. 4
    Sonstigeto afford a crude solid which
  5. 5
    Sonstigeis purified by flash column chromatography on silica gel (100% to 70% hexane/ethyl acetate eluant ratio)

Vorschrift

To a solution of 3-(2′,4′-dichloro-4-ethylbiphen-3-yl)-bicyclo[3.2.1]octane-2,4-dione (0.133 g, 0.34 mmol) in dichloromethane (2 ml) is added triethylamine (0.24 ml, 1.72 mmol) followed by stirring at room temperature for 5 minutes. To this solution is added methyl chloroformate (0.132 ml, 1.72 mmol) dropwise, then the mixture is left to stand overnight. The reaction mixture is concentrated in vacuo to afford a crude solid which is purified by flash column chromatography on silica gel (100% to 70% hexane/ethyl acetate eluant ratio) to afford carbonic acid 3-(2′,4′-dichloro-4-ethylbiphen-3-yl)-4-oxo-bicyclo[3.2.1]oct-2-en-2-yl ester methyl ester.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08828908B2uspto-grants-2014_09