Reaktion #1835764

ord-02ca3153db0340a9b9392d8df166cde7

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter completion of the reaction
  2. 2
    Sonstigethe solvent and trifluoroacetic acid were evaporated
  3. 3
    SonstigeThe obtained residue was purified with silica gel column chromatography (n-hexane:ethyl acetate)

Vorschrift

To 8-(5-bromopyridin-2-yl)-1,4-dioxaspiro[4.5]decane-8-carbonitrile (3.4 g) described in Reference Example 82 was added trifluoroacetic acid (4.1 ml) at room temperature, and stirred at the same temperature for 22 hours. After completion of the reaction, the solvent and trifluoroacetic acid were evaporated. The obtained residue was purified with silica gel column chromatography (n-hexane:ethyl acetate) to give 1-(5-bromopyridin-2-yl)-4-oxocyclohexanecarbonitrile (2.78 g) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09150555B2uspto-grants-2015_10