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

HRID 2236011
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2236011
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 3939Lithium HydroxideHCID 86211537HCID 86211537, Verbindung

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 22242641Methanol--water (1/1)Lösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-a539d314b61e4ee285a086d477bae251
Quelldatensatz
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07713957B2

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