Reaktion #42021

Reaktionsgleichung

KMnO4

ethyl chrysanthemumate

potassium permanganate

acetone

KMnO4

KMnO4

→

caronic acid

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationfiltered
2. 2
   WaschenThe solid cake was washed with acetone (450 mL) and suction
3. 3
   Sonstigedried
4. 4
   workup.ADDITIONThe dried solid was mixed with sodium sulfite (Na2SO3) (364.3 g)
5. 5
   workup.ADDITIONthe solid mixture was added in portions to 30% sulfuric acid (H2SO4) (960 mL)
6. 6
   Temperaturwhile maintaining the temperature below 65° C
7. 7
   workup.ADDITIONEthyl acetate (EtOAc) (1000 mL) was added
8. 8
   Filtrationthe mixture was filtered through celite
9. 9
   SonstigeThe layers were separated
10. 10
    Waschenthe aqueous layer was washed with EtOAc (600 mL)
11. 11
    TrocknenThe combined organic solutions were dried over anhydrous sodium sulfate
12. 12
    Einengenconcentrated to an oil (158.6 g)
13. 13
    workup.ADDITIONThis oil was treated with 45% sodium hydroxide solution (NaOH) (240 mL) and water (100 mL) at 85° C. for about 30 min
14. 14
    TemperaturThe reaction mixture was cooled
15. 15
    Extraktionfurther extracted three times with EtOAc (450 mL)
16. 16
    TrocknenThe combined organic layers were dried over anhydrous sodium sulfate
17. 17
    Einengenconcentrated

Vorschrift

To a solution of ethyl chrysanthemumate (163.1 g) in acetone (600 mL) at 20° C. was added potassium permanganate (KMnO4) (472.7 g) as a solid in 9 equal portions. After each addition of KMnO4, the exotherm that ensued was allowed to subside before the addition of the next portion of KMnO4. Upon completion of KMnO4 addition, the reaction mixture was stirred for another 2 hours and then filtered. The solid cake was washed with acetone (450 mL) and suction dried. The dried solid was mixed with sodium sulfite (Na2SO3) (364.3 g), and the solid mixture was added in portions to 30% sulfuric acid (H2SO4) (960 mL) while maintaining the temperature below 65° C. Ethyl acetate (EtOAc) (1000 mL) was added, and the mixture was filtered through celite. The layers were separated and the aqueous layer was washed with EtOAc (600 mL). The combined organic solutions were dried over anhydrous sodium sulfate and concentrated to an oil (158.6 g). This oil was treated with 45% sodium hydroxide solution (NaOH) (240 mL) and water (100 mL) at 85° C. for about 30 min. The reaction mixture was cooled, acidified to pH 3 with 30% sulfuric acid (about 300 mL) and further extracted three times with EtOAc (450 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated to give caronic acid (162.6 g) as a mixture of cis- and trans-isomers. 1H NMR (400 MHz, CD3OD); cis-isomer δ1.26 (s, 3H), 1.40 (s, 3H), 1.96 (s, 2H); trans-isomer δ1.32 (s, 6H), 2.19 (s, 2H).

Quelle