Reaktion #2137641

Reaktionsgleichung

ammonia

sodium

1,1-ethylenedioxy-4-(1-pentynyl)cyclohexane

ammonia

→

4-(trans-1-pentenyl)cyclohexanone

Ausbeute 83.5%

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeprovided with a magnetic stirrer
2. 2
   Sonstigewas removed by evaporation
3. 3
   workup.WAITleft
4. 4
   SonstigeThe mixture was then partitioned three times in water/diethyl ether
5. 5
   ExtraktionThe aqueous phases were back-extracted with diethyl ether
6. 6
   TrocknenThe organic phases were dried over magnesium sulphate
7. 7
   Sonstigefreed from solvent on a rotary evaporator
8. 8
   workup.ADDITIONThe resulting, pale yellow liquid (3.8 g) was treated with 200 ml of acetone and 0.1 ml of concentrated sulphuric acid
9. 9
   TemperaturThe mixture was heated
10. 10
    Temperaturto reflux for 10 minutes
11. 11
    workup.ADDITIONtreated with water
12. 12
    Sonstigefreed from acetone on a rotary evaporator
13. 13
    SonstigeThe residue was partitioned three times in methylene chloride/water
14. 14
    ExtraktionThe aqueous phases were back-extracted with methylene chloride
15. 15
    TrocknenThe organic phases were dried over magnesium sulphate
16. 16
    Sonstigeevaporated
17. 17
    SonstigeChromatographic separation of the resulting, yellow liquid (3.5 g) on silica gel with ethyl acetate/petroleum ether (vol. 7:93)

Vorschrift

A solution of 4.5 g of 1,1-ethylenedioxy-4-(1-pentynyl)cyclohexane in 54 ml of tetrahydrofuran was treated dropwise with about 50 ml of pre-condensed ammonia in a sulphonation flask provided with a magnetic stirrer. The mixture was subsequently treated portionwise at -78° C. within 7 hours with 1.3 g of sodium. 1.5 hours after the last addition the ammonia was removed by evaporation and the mixture was neutralized with 25% hydrochloric acid and left to stand overnight. The mixture was then partitioned three times in water/diethyl ether. The aqueous phases were back-extracted with diethyl ether. The organic phases were dried over magnesium sulphate and then freed from solvent on a rotary evaporator. The resulting, pale yellow liquid (3.8 g) was treated with 200 ml of acetone and 0.1 ml of concentrated sulphuric acid. The mixture was heated to reflux for 10 minutes, then treated with water and freed from acetone on a rotary evaporator. The residue was partitioned three times in methylene chloride/water. The aqueous phases were back-extracted with methylene chloride. The organic phases were dried over magnesium sulphate and evaporated. Chromatographic separation of the resulting, yellow liquid (3.5 g) on silica gel with ethyl acetate/petroleum ether (vol. 7:93) gave 3.0 g (83.5%) of 4-(trans-1-pentenyl)cyclohexanone as a pale yellow liquid.

Quelle