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Acetic Anhydride → (2S)-2-acetamido-3,3-dimethylbutanoic acid

HRID 1260130
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1260130
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([CH3:6])([CH3:5])[CH3:4].[C:10](OC(=O)C)(=[O:12])[CH3:11]>C(O)(=O)C>[C:10]([NH:1][C@H:2]([C:7]([OH:9])=[O:8])[C:3]([CH3:6])([CH3:5])[CH3:4])(=[O:12])[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7918Acetic AnhydrideHCID 164608L-tert-Leucine

Produkt 1

HCID 11469346(2S)-2-acetamido-3,3-dimethylbutanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

L-tert-Leucine (manufactured by Tokyo Kasei Kogyo) (4.7 g) was suspended in glacial acetic acid (manufactured by Nakarai Tesk, 40 mL) and heated at 40 to 50° C. together with addition of thrice molar acetic acid anhydride (manufactured by Nakarai Tesk) thereto whereupon the reaction was conducted. After glacial acetic acid was removed in vacuo, the crude crystals were obtained. After that, the crude crystals were recrystallized from 20% isopropyl alcohol. The precipitate was ground in a mortar and dried to give powder of N-acetyl-L-tert-leucine. Details thereof are mentioned in J. P. Greenstein, Chemistry of Amino Acids, 1961, 3.

Aufarbeitung

  1. customAfter glacial acetic acid was removed in vacuo
  2. customthe crude crystals were obtained
  3. customAfter that, the crude crystals were recrystallized from 20% isopropyl alcohol
  4. customdried

Quellen und Nachweise

ORD-Eintrag
ord-e27cb2b771654a50b7c924b34b8ba222
Quelldatensatz
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08470574B2

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