Реакция #569308

ord-3a915aac78f24bb3ba0b12eecf7d906b

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooling
  2. 2
    КонцентрированиеAt 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
    Концентрированиеwas then concentrated by evaporation under reduced pressure
  5. 5
    Другоеfinally dried sufficiently in vacuo
  6. 6
    ДругоеThe whole of the resulting crude trifluoroacetyl compound was used in the subsequent step (b) without purification

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05792840uspto-grants-1998_08