Reaktion #1793

ord-e3ff06e7d5dc4790a4038ff5d1f041f4

Reaktionsgleichung

O=S(=O)=c1cc(O)cco1
sulfonylpyran-4-ol
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
C1CCOC1
THF
COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
C1CCOC1
THF
COC(=O)c1ccc(OC(=O)c2cc(=S(=O)=O)cco2)cc1OC
methyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoate

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (364 mg, 2.0 mmol) in dry THF (4 mL) was added triphenylphosphine (524.6 mg, 2.0 mmol) and the solution was cooled to 0° C. A 2.5 mL volume of sulfonylpyran-4-ol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 μL, 2.0 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-sulfonylpyranoyloxy]-2-methoxybenzoate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726172uspto-grants-1998_03