Réaction #1770

ord-2e02459c44114d51802676f652203008

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe reaction was filtered
  2. 2
    Autrethe solvent was removed under reduced pressure
  3. 3
    AutreThe residue was chromatographed on a silica gel column
  4. 4
    LavageEtOAc and eluted with same
  5. 5
    Autrethe solvent removed under reduced pressure

Mode opératoire

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (713 mg, 3.92 mmol) in dry THF (7.5 mL) was added triphenylphosphine (1.42 g, 5.4 mmol) and the solution was cooled to 0° C. A 2.5 mL volume of tetrahydro-4H-pyran-4-ol (466 mL, 4.90 mmol) and diethyl azodicarboxylate (850 μL, 5.4 mmol) in THF was added dropwise via addition funnel over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 60:40 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05726172uspto-grants-1998_03