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Sulfuric Acid → N-methylaspartic acid sulfate

HRID 39211
ノート
印刷プレビュー

反応式

HRID 39211 の反応式
[CH3:1][NH:2][C@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5]([OH:7])=[O:6].[S:11](=[O:15])(=[O:14])([OH:13])[OH:12]>O>[S:11]([OH:15])([OH:14])(=[O:13])=[O:12].[CH3:1][NH:2][C@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5]([OH:7])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1118Sulfuric AcidHCID 92982N-Methyl-L-aspartic acid

生成物 1

HCID 86639894N-methylaspartic acid sulfate収率 95.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

10.7 g of N-methylaspartic acid was placed in a 250 ml round-bottom flask, and 100 ml of water was added to the flask and stirred for 30 minutes by using a magnetic stirrer. 7.12 g of concentrate sulfuric acid (concentration: 98%) was slowly dropped into the flask under stirring, and stirred for additional 2 hours after dropping. After the reaction, the reaction solution was concentrated, azeotroped with 100 ml of toluene to further remove the water and dried under vacuum to obtain 17 g of N-methylaspartic acid sulfate as yellow oil (Yield: 95.3%).

後処理

  1. stirringunder stirring
  2. stirringstirred for additional 2 hours
  3. customAfter the reaction
  4. concentrationthe reaction solution was concentrated
  5. customazeotroped with 100 ml of toluene
  6. customto further remove the water
  7. customdried under vacuum

出典と根拠

ORDレコード
ord-53db3abe415442db8d58a89781f64b4c
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08524895B2

反応ノート

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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