Реакция #49636

Уравнение реакции

hydrogen chloride

hydrogen

1-(2-bicyclo [2.2.2] octyl)-1-(trimethylphenyl)-ethane

1-(2-bicyclo [2.2.2] octyl)-1-(trimethylcyclohexyl)-ethane

→

1,2,4-trimethylbenzene

Растворители

methylcyclohexane

Условия реакции

Обработка

1. 1
   workup.ADDITIONabove was dropped
2. 2
   ДругоеThe so obtained mixture
3. 3
   Температураwas maintained at 30° C. in an ice-cold water bath
4. 4
   workup.STIRRINGfurther stirred for 30 minutes
5. 5
   Другоеthe reaction
6. 6
   Другоеan organic layer produced
7. 7
   Промывкаtherein was washed twice with 200 ml of 2N NaOH aqueous solution
8. 8
   Промывкаby washing twice with 200 ml of water
9. 9
   workup.ADDITIONThe so treated organic layer
10. 10
    Сушкаwas dried with anhydrous MgSO4
11. 11
    workup.DISTILLATIONdistilled
12. 12
    Другоеto obtain 180 g of a fraction
13. 13
    ДругоеThe analysis with NMR and MS resulted in a finding that the so obtained reaction product
14. 14
    Другоеreaction product
15. 15
    workup.ADDITIONwere added
16. 16
    Другоеa reaction temperature of 200° C.
17. 17
    Другоеa reaction time of 6 hours
18. 18
    ДругоеThe so obtained
19. 19
    Другоеreaction product
20. 20
    Другоеresulting in a finding that it
21. 21
    ДругоеFurther, the traction coefficient of the obtained reaction product
22. 22
    Другоеwas determined in a temperature range of 40° C. to 140° C.

Методика

In a 2 liter four neck flask equipped with a thermometer and a hydrogen chloride gas trap, 500 ml of 1,2,4-trimethylbenzene and 150 ml of titanium tetrachloride were placed and 150 ml of 2-(1-hydroxyethyl) bicyclo [2.2.2] octane obtained in (1) above was dropped therein over 30 minutes with stirring at room temperature. The so obtained mixture was maintained at 30° C. in an ice-cold water bath and further stirred for 30 minutes. After the evolution of hydrogen chloride gas was stopped, the content of the flask was poured into 1 liter of ice-cold water to stop the reaction. The mixture was stirred well in the ice-cold water, and an organic layer produced therein was washed twice with 200 ml of 2N NaOH aqueous solution, followed by washing twice with 200 ml of water. The so treated organic layer was dried with anhydrous MgSO4 and distilled to obtain 180 g of a fraction having a boiling point of 150 to 160° C./2 mmHg. The analysis with NMR and MS resulted in a finding that the so obtained reaction product was 1-(2-bicyclo [2.2.2] octyl)-1-(trimethylphenyl)-ethane. Said reaction product was placed in a 1 liter autoclave, 20 g of 5% ruthenium/carbon catalyst and 300 ml of methylcyclohexane as the solvent were added and the resulting mixture was hydrogenated under the conditions of a hydrogen pressure of 80 kg/cm2G, a reaction temperature of 200° C. and a reaction time of 6 hours. The NMR analysis showed that the degree of hydrogenation was 99%. The so obtained reaction product was analyzed with NMR, IR and MS, resulting in a finding that it was 1-(2-bicyclo [2.2.2] octyl)-1-(trimethylcyclohexyl)-ethane. Further, the traction coefficient of the obtained reaction product was determined in a temperature range of 40° C. to 140° C. and the results are shown in FIG. 1. The graphs of 1H-NMR, 13C-NMR and MS of the reaction product are respectively shown in FIGS. 4 to 6.

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