Réaction #955942

ord-7dc18e094ee14c86a438c03c7b3044c6

Équation de réaction

CSCC[C@H](N)C(=O)O
methionine
CSCCC1NC(=O)C(CCSC)NC1=O
Bis[2-(methylthio)ethyl]-2,5-piperazinedione
CSCCC1NC(=O)C(CCSC)NC1=O
3,6-bis[2-(methylthio)ethyl]-2,5-piperazinedione

Réactifs

Aucun

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGstirred at 160° C. for 6 hours, during which the pressure
  2. 2
    Températureincreased to 15 bar
  3. 3
    TempératureThe autoclave was then cooled in an ice bath
  4. 4
    Filtrationthe resulting suspension was filtered
  5. 5
    Lavagethe solid was washed with 75 ml of water
  6. 6
    AutreFinally, the solid was dried in a vacuum
  7. 7
    Autredrying oven at 50° C. overnight

Mode opératoire

A suspension of 13.4 g (0.09 mol) of methionine, 17.2 g (0.09 mol, purity: 91%) of methioninehydantoin (IId) and 150 g of water were introduced into a 200 ml Roth steel autoclave with magnetic stirring and stirred at 160° C. for 6 hours, during which the pressure increased to 15 bar. From time to time, the autoclave was decompressed until the pressure settled at a constant 10 bar. The autoclave was then cooled in an ice bath, and the resulting suspension was filtered and the solid was washed with 75 ml of water. Finally, the solid was dried in a vacuum drying oven at 50° C. overnight. Bis[2-(methylthio)ethyl]-2,5-piperazinedione (III) was isolated as yellowish white crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08968817B2uspto-grants-2015_03