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HCID 86750087, Verbindung → (+)-cis-4-Amino-1-benzyl-3-methyl-2-oxopyrrolidine

HRID 378568
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 378568
[CH2:1]([N:8]1[CH2:12][C@H:11]([NH:13]C(OC(C)(C)C)=O)[C@H:10]([CH3:21])[C:9]1=[O:22])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[NH2:13][C@H:11]1[CH2:12][N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:9](=[O:22])[C@H:10]1[CH3:21]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 86750087HCID 86750087, Verbindung

Produkt 1

HCID 68547926(+)-cis-4-Amino-1-benzyl-3-methyl-2-oxopyrrolidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

In 15 ml of trifluoroacetic acid was dissolved 1.76 g of Compound (44). After 1 hour, the solution was concentrated under reduced pressure. To the residue was added 100 ml of water, and the mixture was washed with benzene. The aqueous layer was adjusted to a pH of 12 with sodium hydroxide and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated to obtain the titled compound (45) as a colorless oil.

Aufarbeitung

  1. concentration
the solution was concentrated under reduced pressure
  • additionTo the residue was added 100 ml of water
  • washthe mixture was washed with benzene
  • extractionextracted with chloroform
  • dry with materialThe organic layer was dried over anhydrous sodium sulfate
  • customthe solvent was evaporated
  • Quellen und Nachweise

    ORD-Eintrag
    ord-23ccee669d674019844fa538b3a998e4
    Quelldatensatz
    uspto-grants-2000_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06031102

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