Reaktion #569308

ord-3a915aac78f24bb3ba0b12eecf7d906b

Reaktionsgleichung

Cl.N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
D-(+)-glucosamine hydrochloride
CCN(CC)CC
triethylamine
CCOC(=O)C(F)(F)F
ethyl trifluoroacetate
O=C(N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(F)(F)F
N-Trifluoroacetylglucosamine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooling
  2. 2
    EinengenAt the end of this time, the mixture was concentrated by evaporation under reduced pressure
  3. 3
    workup.ADDITIONbenzene (250 ml twice) and ethyl acetate (250 ml) were repeatedly added to the residue, which
  4. 4
    Einengenwas then concentrated by evaporation under reduced pressure
  5. 5
    Sonstigefinally dried sufficiently in vacuo
  6. 6
    SonstigeThe whole of the resulting crude trifluoroacetyl compound was used in the subsequent step (b) without purification

Vorschrift

160 g (0.742 mole) of D-(+)-glucosamine hydrochloride were dissolved in 2200 ml of methanol (99.6% purity), and 187.9 g (1.86 mole) of triethylamine were added to the resulting solution. 115.9 g of ethyl trifluoroacetate were then added dropwise to the resulting mixture, whilst ice-cooling, after which the mixture was stirred overnight at room temperature. At the end of this time, the mixture was concentrated by evaporation under reduced pressure, and then benzene (250 ml twice) and ethyl acetate (250 ml) were repeatedly added to the residue, which was then concentrated by evaporation under reduced pressure and then finally dried sufficiently in vacuo. The whole of the resulting crude trifluoroacetyl compound was used in the subsequent step (b) without purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05792840uspto-grants-1998_08