Réaction #674319

ord-6796e4ab1c0444cba33a0d3bcfbade61

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionthe solution was extracted with aqueous 3N NaOH
  2. 2
    LavageThe organic layer was washed with brine
  3. 3
    Séchagedried over MgSO4
  4. 4
    Concentrationconcentrated in vacuo

Mode opératoire

To an ice-cold solution of the compound from Step 1 (2.60 g, 12.9 mmol), phenol (3.64 g, 38.7 mmol), and triphenylphosphine (6.77 g, 25.8 mmol) in DCM (50 mL) was added a solution of diisopropyl azodicarboxylate (5.22 g, 25.8 mmol) in toluene (30 mL). After stirring at room temperature for 60 hours it was diluted with ether and the solution was extracted with aqueous 3N NaOH. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The intermediate tert-butyl (R)-2-(phenoxymethyl)pyrrolidine-1-carboxylate was obtained from the residue by column chromatography (silica gel, cHex/EtOAc 29:1); yield: 1.82 g (51%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09226929B2uspto-grants-2016_01