Reaktion #1268201

ord-24962bd0b77a44abb36e23851cb56731

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to ambient temperature
  2. 2
    EinengenAfter concentrating the reaction mixture under reduced pressure, DI water
  3. 3
    workup.ADDITIONwas added (100 mL)
  4. 4
    SonstigeThe reaction mixture was partitioned between water and CH2Cl2 (200 mL)
  5. 5
    WaschenThe organic phase was washed with 1N HCl (50 mL)
  6. 6
    Trocknendried (MgSO4)
  7. 7
    Filtrationfiltered
  8. 8
    Einengenconcentrated
  9. 9
    SonstigeThe material was used without further purification

Vorschrift

2-(3-Phenyl-propionylamino)-succinic acid 4-methyl ester (10 g, 36 mmol), pyridine (50 mL) and acetic anhydride (45 mL) were combined in a 500 mL flask. The reaction mixture was heated at 90° C. for 2 h and then cooled to ambient temperature. After concentrating the reaction mixture under reduced pressure, DI water was added (100 mL). The reaction mixture was partitioned between water and CH2Cl2 (200 mL). The organic phase was washed with 1N HCl (50 mL), dried (MgSO4), filtered, and concentrated. The material was used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.31-7.20 (m, 5H), 6.79 (br d, J=7.6 Hz, 1H), 4.72 (X of ABX, 1H), 3.65 (s, 3H), 3.01-2.93 (m, 3H), 2.71-2.62 (m, 3H), 2.11 (s, 3H); MS (EI) 278.1 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07282501B2uspto-grants-2007_10