Reaktion #1365697

ord-86563f1273724ae28f3453b117a169f3

Reaktionsgleichung

O=C1O[C@H]([C@@H](O)CO)C(O)=C1O
Ascorbic acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
BrCc1ccccc1
benzyl bromide
O=C1O[C@H]([C@@H](O)CO)C(OCc2ccccc2)=C1O
3-O-benzyl ascorbic acid
Ausbeute 48.0%

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled down to the room temperature
  2. 2
    Sonstigeto produce a solid
  3. 3
    FiltrationAfter filtration
  4. 4
    Einengenthe filtrate was concentrated under reduced pressure
  5. 5
    Sonstigepurified by column chromatography on silica gel

Vorschrift

Ascorbic acid (10 g, 56.8 mmol) was dissolved in 60 ml of dimethylsulfoxide, followed by addition of cesium carbonate (9.25 g, 28.4 mmol). After 20 minutes, benzyl bromide (6.75 ml, 56.8 mmol) was added to the reaction mixture and heated to 50° C. for 18 hours. The reaction mixture was cooled down to the room temperature and diluted with 150 ml of dichloromethane to produce a solid. After filtration, the filtrate was concentrated under reduced pressure and purified by column chromatography on silica gel to give 7.2 g of the 3-O-benzyl ascorbic acid (yield 48%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06444144B1uspto-grants-2002_09