Acetic-formic anhydride → Ethyl N-formyl-3-nitriloalaninate

HRID 1674707Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1674707
[N:1]#[C:2][C@@H:3]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[NH2:4].[CH:10](OC(=O)C)=[O:11]>CCOCC>[CH:10]([NH:4][C@H:3]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[C:2]#[N:1])=[O:11]

Komponenten

4

Edukt 2

HCID 75269Acetic-formic anhydrideHCID 931182Ethyl 3-nitriloalaninate

Produkt 1

HCID 86619658Ethyl N-formyl-3-nitriloalaninate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

Ethyl 3-nitriloalaninate (26.9 g, 210 mmol) is dissolved in anhydrous ether (200 mL), and cooled in an ice/water bath. Acetic formic anhydride (prepared as a mixture as described above) is added dropwise. When the addition is finished, the reaction mixture is allowed to warm to RT and stirred at RT overnight. Most volatiles are removed in vacuo, and the residue solvents are removed by co-evaporation with toluene (100 mL×4). The red oil obtained precipitates upon scratching in ether, and the resulting solids are recrystallized in ether to give the title compound as a white solid. 1H NMR (400 MHz, CDCl3) 8.32 (1H, s), 7.26 (1H, s), 6.46 (1H, bs), 5.56 (1H, d, J 7.8), 4.39 (2H, q), 1.37 (3H, t).

Aufarbeitung

  1. temperaturecooled in an ice/water bath
  2. additionis added dropwise
  3. additionWhen the addition
  4. customMost volatiles are removed in vacuo
  5. customthe residue solvents are removed by co-evaporation with toluene (100 mL×4)
  6. customThe red oil obtained
  7. customprecipitates
  8. customthe resulting solids are recrystallized in ether

Quellen und Nachweise

ORD-Eintrag
ord-572de257db494463bbdbf9584753597d
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08003656B2

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