Реакция #1178389

Уравнение реакции

hydrogen peroxide

sulphuric acid

2,5-dimethyl-2,5-hexanediol

→

2,5-dimethyl-2,5-di(tert-butylperoxy)hexane

Выход 90.0%

Растворители

water

Условия реакции

Обработка

1. 1
   Другоеwere metered in within 60 min, in the course of which
2. 2
   Другоеrose from 20° C. to 30-32° C
3. 3
   workup.STIRRINGThe reaction mixture was stirred at 30° C. for another 90 min
4. 4
   Другоеthe suspension formed
5. 5
   Фильтрацияwas filtered within 10 min
6. 6
   Фильтрацияto the filtration devices (5)
7. 7
   Промывкаwas washed
8. 8
   workup.ADDITIONby adding 500 kg of water
9. 9
   workup.STIRRINGstirring the suspension for 3 min
10. 10
    Фильтрацияfiltering again
11. 11
    Фильтрацияto the filtration devices (5)
12. 12
    workup.ADDITIONThereafter, 481 kg of tert-butanol were added
13. 13
    workup.DISSOLUTIONthe solid was dissolved
14. 14
    workup.STIRRINGby stirring
15. 15
    Температураheating
16. 16
    workup.STIRRINGwith stirring
17. 17
    Температураcooling of the reactor through the jacket, in the course of which the temperature
18. 18
    Другоеrose to from 40 to 45° C
19. 19
    workup.STIRRINGThe reaction mixture was stirred at this temperature for a further 60 min
20. 20
    ДругоеThe lower aqueous phase was removed
21. 21
    Промывкаthe liquid product was washed successively with 150 kg of water, 150 kg of 1% by weight sodium hydroxide solution and 150 kg of water
22. 22
    workup.STIRRINGby stirring the phases
23. 23
    Другоеremoving the lower aqueous phase
24. 24
    ДругоеAfter removal of residual water and volatile by-products

Методика

A reactor corresponding to FIG. 1 was initially charged with a mixture of 550 kg of 70% by weight hydrogen peroxide and 366 kg of 80% by weight sulphuric acid. With stirring and cooling of the reactor through the jacket, 250 kg of 2,5-dimethyl-2,5-hexanediol were metered in within 60 min, in the course of which the temperature rose from 20° C. to 30-32° C. The reaction mixture was stirred at 30° C. for another 90 min and then admixed with 200 kg of water. The stirrer was then switched off and the suspension formed was filtered within 10 min by applying reduced pressure to the filtration devices (5), in the course of which the liquid phase was sucked into the collecting vessel (7) and the precipitated 2,5-dimethylhexane-2,5-dihydroperoxide was retained in the vessel (2). The solid product retained in the reactor was washed by adding 500 kg of water, stirring the suspension for 3 min and filtering again by applying reduced pressure to the filtration devices (5). This washing operation was repeated once more. Thereafter, 481 kg of tert-butanol were added and the solid was dissolved therein by stirring and heating. 500 kg of 80% by weight sulphuric acid were metered into the resulting solution within 60 min with stirring and cooling of the reactor through the jacket, in the course of which the temperature rose to from 40 to 45° C. The reaction mixture was stirred at this temperature for a further 60 min and then admixed with 50 kg of water. The lower aqueous phase was removed and the liquid product was washed successively with 150 kg of water, 150 kg of 1% by weight sodium hydroxide solution and 150 kg of water, by stirring the phases and then removing the lower aqueous phase. After removal of residual water and volatile by-products by stripping under reduced pressure in a stripping column, 405 kg (90%) of 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane were obtained.

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