Reaktion #930544

ord-de78dc77af144fa69f11023380cf6f55

Reaktionsgleichung

CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)C[C@@H](O)CC2(C)C)C(C)(C)C[C@H](O)C1
Zeaxanthin
[Na+].[O-][Br+2]([O-])[O-]
sodium bromate
[Br-].[K+]
potassium bromide
O=S(=O)(O)O
sulfuric acid
[Na+].[OH-]
sodium hydroxide
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)C(=O)[C@@H](O)CC2(C)C)C(C)(C)C[C@H](O)C1=O
astaxanthin
Ausbeute 28.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled on ice
  2. 2
    workup.ADDITIONwas added rapidly
  3. 3
    Sonstigethe reaction
  4. 4
    FiltrationThe mixture was filtered over celite
  5. 5
    Sonstigethe phases were separated
  6. 6
    WaschenThe organic layer was washed with basic water
  7. 7
    Sonstigeseparated
  8. 8
    SonstigeThe chloroform was removed under vacuum at around 40° C. until a thick slurry
  9. 9
    workup.ADDITIONEthanol (90 ml) was added
  10. 10
    Sonstigethe remaining chloroform was removed by vacuum distillation
  11. 11
    TemperaturThe reaction mixture was cooled
  12. 12
    Filtrationthe product collected by filtration

Vorschrift

Zeaxanthin (6.24 gm, 11 mmole) was slurried in 110 ml of chloroform under nitrogen and cooled on ice. To this stirred mixture, was added a solution of 6.14 gm (51.6 mmole) sodium bromate in 35 ml of water and acidified with 1 ml of 50% sulfuric acid. The three phase mixture was cooled on ice and 4 ml of a solution containing 4.84 gm (32.1 mmole) of potassium bromide in 15 ml of water was added rapidly to begin the reaction. After 1 hour, 7 ml of 3 N sodium hydroxide was added and the mixture was stirred for 15 minutes. The mixture was filtered over celite and the phases were separated. The organic layer was washed with basic water and separated. The chloroform was removed under vacuum at around 40° C. until a thick slurry remained. Ethanol (90 ml) was added and the remaining chloroform was removed by vacuum distillation. The reaction mixture was cooled and the product collected by filtration to yield 1.78 grams (28.5% yield) astaxanthin.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06376717B2uspto-grants-2002_04