Reaction #595304

ord-6ccbbcd80090488ea5d8a7c08c1cd5be

Reaction equation

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

Reagents

None

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.v1Patent: US09095161B2uspto-grants-2015_08