Reaktion #1778

ord-c76a22e184294ef893b6fc5df9e611d7

Reaktionsgleichung

OC1CCOc2ccccc21
4-chromanol
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate

Lösungsmittel

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 (1.25 mL) was added triphenylphosphine (525 mg, 2.0 mmol) and the solution was cooled to 0° C. A 500 mL volume of 4-chromanol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 mL, 2.0 mmol) in THF was added dropwise via syringe 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 92:8 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-(4-chromanoyloxy)-2-methoxybenzoate.

Quelle

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