Reaktion #725754

ord-7fb0fffaef3445019651c8328efcf474

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONdissolved
  2. 2
    FiltrationThe precipitated solid was filtered
  3. 3
    workup.DISSOLUTIONdissolved in Et2O (1500 ml)
  4. 4
    WaschenThe organic phase was washed with water until neutral, saturated NaCl
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Einengenconcentrated in vacuo

Vorschrift

Finely powdered isopropyl[3-(4-methoxybenzoyl)-1,2,4-oxadiazol-5-yl]acetate (13.5 g) was added in portions over 15 minutes to concentrated H2SO4 (1000 ml) with mechanical stirring. The mixture was stirred an additional 15 minutes until the ester dissolved. The resulting solution was added slowly to ice water (6 liters) with stirring. The precipitated solid was filtered and dissolved in Et2O (1500 ml). The organic phase was washed with water until neutral, saturated NaCl, dried over Na2SO4, and concentrated in vacuo to give 11.0 g of an amorphous solid. The crude acid (7.7 g) was triturated with boiling Et2O (500 ml) to give 3.6 g (45%) of a powder, m.p. 126°-127°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04562186uspto-grants-1985_12