تفاعل #328649

معادلة التفاعل

1-methylcyclohexanol

hydrogen peroxide

→

Di(1-methyl-cyclohexyl)peroxide

ظروف التفاعل

المعالجة

1. 1
   أخرىto give a viscous brown mixture
2. 2
   غسيلrinsed with water
3. 3
   workup.ADDITIONadded dropwise
4. 4
   أخرىThe solution separated into two phases
5. 5
   workup.ADDITIONCyclohexanol (150 mL) was added
6. 6
   أخرىthe mixture was transferred to a separating funnel
7. 7
   استخلاصThe aqueous fraction was extracted with another portion of cyclohexane (150 ml)
8. 8
   غسيلthe combined organic fractions washed with 1M NaOH (2×100 mL), water (2×150 mL)
9. 9
   أخرىdried
10. 10
    أخرىevaporated
11. 11
    أخرىto give a viscous colourless oil
12. 12
    غسيلeluted with cyclohexane
13. 13
    أخرىAfter evaporation at reduced pressure 0.7 g colourless oil of di(1-methyl-cyclohexyl)peroxide
14. 14
    أخرىwas obtained

الإجراء التجريبي

1-methylcyclohexanol (30 g, 0.26 mol) was placed in a 100 mL three necked round bottomed flask and was stirred. The flask was cooled in a brine/ice bath, dropping funnel fitted and fitted with a static N2 supply. The dropping funnel was charged with 98% sulfuric acid (16.14 ml) and water (6.45 ml) giving a 70% sulfuric acid solution. This was added dropwise to the 1-methylcyclohexanol and stirring continued to give a viscous brown mixture. The bath was recharged with ice/brine, dropping funnel rinsed with water and recharged with 35% hydrogen peroxide (6.98 mL, 0.125 mol) and added dropwise. The solution separated into two phases. Cyclohexanol (150 mL) was added and the mixture was transferred to a separating funnel. The aqueous fraction was extracted with another portion of cyclohexane (150 ml) and the combined organic fractions washed with 1M NaOH (2×100 mL), water (2×150 mL), dried and evaporated to give a viscous colourless oil. (12.98 g). The oil was sorbed onto silica gel then placed on a silica gel column and eluted with cyclohexane. After evaporation at reduced pressure 0.7 g colourless oil of di(1-methyl-cyclohexyl)peroxide was obtained. 13C-NMR (CDCl3) δ 22.45, 25.01, 25.95, 35.39, 78.58

المصدر