Reaktion #4889

ord-b804369893e54bd59770ee9a23839cc6

Reaktionsgleichung

O=C(O)C[C@H](O)C(=O)O
(S)-malic acid
CN
methylamine
CN1C(=O)C[C@H](O)C1=O
(S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeslowly rose to 50° C
  2. 2
    TemperaturAfter 0.5 hr the stirred mixture was heated
  3. 3
    Temperaturto reflux
  4. 4
    Sonstigethe water was collected in a Dean-Stark trap for 48 hours
  5. 5
    SonstigeA total of 93 ml of water was collected
  6. 6
    workup.ADDITIONThe toluene residue was treated with 300 ml of ethanol
  7. 7
    Einengenconcentrated on the rotary evaportor
  8. 8
    workup.DISTILLATIONThe residue was distilled
  9. 9
    SonstigeThe yield of product obtained
  10. 10
    Sonstige145°/0.5 mm

Vorschrift

To a stirred solution of 134 g (1 mole) of (S)-malic acid in 700 ml of toluene was added 97 ml of 40% aqueous methylamine. The temperature slowly rose to 50° C. After 0.5 hr the stirred mixture was heated to reflux and the water was collected in a Dean-Stark trap for 48 hours. A total of 93 ml of water was collected. The toluene residue was treated with 300 ml of ethanol and concentrated on the rotary evaportor. The residue was distilled. The yield of product obtained was 101 g (78%), b.p. 140°/2 mm; 145°/0.5 mm.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04727152uspto-grants-1988_02