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L-Methionine → 3,6-bis[2-(methylthio)ethyl]piperazine-2,5-dione

HRID 508122
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HRID 508122 반응식
[NH2:1][C@H:2]([C:7]([OH:9])=O)[CH2:3][CH2:4][S:5][CH3:6]>O>[CH3:6][S:5][CH2:4][CH2:3][CH:2]1[NH:1][C:7](=[O:9])[CH:2]([CH2:3][CH2:4][S:5][CH3:6])[NH:1][C:7]1=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 6137L-Methionine

생성물 1

HCID 1698423,6-bis[2-(methylthio)ethyl]piperazine-2,5-dione

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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.

후처리

  1. stirringstirred at 160° C. for 6 hours, during which the pressure
  2. temperature
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
increased to 15 bar
  • temperatureThe autoclave was then cooled in an ice bath
  • filtrationthe resulting suspension was filtered
  • washthe solid was washed with 75 ml of water
  • customFinally, the solid was dried in a vacuum
  • customdrying oven at 50° C. overnight
  • 출처 및 근거

    ORD 기록
    ord-6ccbbcd80090488ea5d8a7c08c1cd5be
    출처 데이터셋
    uspto-grants-2015_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09095161B2

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