Reaktion #1835704

ord-e0b9aa11765f420b965e8a0d0d8b7c74

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    WaschenThe organic layer was washed with saturated brine
  3. 3
    Trocknendried over anhydrous sodium sulfate
  4. 4
    Einengenconcentrated

Vorschrift

5-Bromo-2-(1,4-dioxaspiro[4,5]decane-8-yl)pyridine (9.0 g) described in Reference Example 102(2) was dissolved in trifluoroacetic acid (15 ml) and stirred at room temperature overnight. After completion of the reaction, water was added under ice cooling, neutralized by the addition of 4N aqueous solution of sodium hydroxide and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to give 4-(5-bromopyridin-2-yl)cyclohexanone (7.9 g) as a pale yellow solid.

Quelle

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