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

HRID 868760
ノート
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反応式

HRID 868760 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 6137L-Methionine

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  1. stirringstirred at 160° C. for 6 hours, during which the pressure
  2. temperatureincreased to 15 bar
このページの内容参加物実験手順後処理出典と根拠反応ノート
  • 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
  • 出典と根拠

    ORDレコード
    ord-7dc18e094ee14c86a438c03c7b3044c6
    出典データセット
    uspto-grants-2015_03
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08968817B2

    反応ノート

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