Reaktion #439626

ord-56fd7fa0741f4590bc8cbc2b3cab77f3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe mixture was evaporated
  2. 2
    Sonstigethe residue purified by chromatography (SiO2, n-hexane/AcOEt 6:1)

Vorschrift

To a solution of 0.50 g 4-hydrox-phenylaniline, 0.83 g of 2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethan-1-ol and 1.06 g of triphenylphosphine in 20 ml of THF was added at 0° C. a solution of 0.82 g of diisopropyl azodicarboxylate in 10 ml of THF over 30 min and stirring was continued at 22° C. for 5 h. The mixture was evaporated and the residue purified by chromatography (SiO2, n-hexane/AcOEt 6:1) to give 0.62 g of the title compound as a colorless solid. MS: (M+H)+ 371.4.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06747049B2uspto-grants-2004_06