Acetyl chloride → HCID 53239786, Verbindung

HRID 576487Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 576487
[C:1]([NH:4][C@H:5]1[C@H:14]([C@@H:15]([C@@H:17]([CH2:19][OH:20])[OH:18])[OH:16])[O:13][C:8]([OH:12])([C:9](=[O:11])[OH:10])[CH2:7][C@@H:6]1[OH:21])(=[O:3])[CH3:2].[C:22](Cl)(=O)[CH3:23]>C(O)C>[C:1]([NH:4][C@H:5]1[C@H:14]([C@@H:15]([C@@H:17]([CH2:19][OH:20])[OH:18])[OH:16])[O:13][C:8]([OH:12])([C:9](=[O:10])[O:11][CH2:22][CH3:23])[CH2:7][C@@H:6]1[OH:21])(=[O:3])[CH3:2]

Komponenten

4

Versuchsvorschrift

To a suspension of N-acetyl-neuraminic acid (1 g, 3.23 mmole) in anhydrous ethanol (75 ml) was added 1.5 ml acetyl chloride. The mixture was sealed and stirred at room temperature for 16 hrs. to form a clear solution. The resulting solution was vacuum evaporated to dryness. The white solid was washed with ethyl acetate and vacuum dried to afford the title compound as a white solid (1 g, 91.7%).

Aufarbeitung

  1. customThe mixture was sealed
  2. customto form a clear solution
  3. customevaporated to dryness
  4. washThe white solid was washed with ethyl acetate and vacuum
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-7f9e2d549f6443b1a1bdd998a8751f4c
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09040503B2

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