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Lithium Hydroxide → {[(1-Ethyl-1-methylpropoxy)carbonyl]amino}acetic acid

HRID 2374830
ノート
印刷プレビュー

反応式

HRID 2374830 の反応式
[CH2:1]([C:3]([CH3:16])([O:6][C:7]([NH:9][CH2:10][C:11]([O:13]CC)=[O:12])=[O:8])[CH2:4][CH3:5])[CH3:2].[OH-].[Li+]>CO.O>[CH2:1]([C:3]([CH3:16])([O:6][C:7]([NH:9][CH2:10][C:11]([OH:13])=[O:12])=[O:8])[CH2:4][CH3:5])[CH3:2]
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 3939Lithium HydroxideHCID 86211537HCID 86211537、化合物

生成物 1

HCID 85792234{[(1-Ethyl-1-methylpropoxy)carbonyl]amino}acetic acid

試薬・触媒・溶媒 1

HCID 22242641Methanol--water (1/1)溶媒

実験手順

300 mg (1.30 mmol) of ethyl {[(1-ethyl-1-methylpropoxy)carbonyl]-amino}acetate was dissolved in 2.5 ml of a solvent mixture of methanol:water (2.3:1). 1.56 ml of 1 N aqueous lithium hydroxide solution was added to the obtained solution. After stirring at room temperature for 2 hours, “DOWEX” (50W-X2 100 to 200 mesh H form) (an exchange resin of The Dow Chemical Company) was added to the reaction mixture under gentle stirring until pH of the mixture had become 5. The resin was obtained by the filtration under suction and then the filtrate was concentrated under reduced pressure and then dried to obtain the title compound.

後処理

  1. additionwas added to the reaction mixture
  2. stirringunder gentle stirring until pH of the mixture
  3. customThe resin was obtained by the filtration under suction
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customdried

出典と根拠

ORDレコード
ord-d11e64fb30a440ad8aa162788b05b194
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07462630B2

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