Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Alpha-Methylstyrene | HCID 7407 | — |
| Reactant | tert-Amyl hydroperoxide | HCID 76962 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cumyl t-amyl peroxide | HCID 18979329 | 60.5% |
Reaction Steps
Into the 200 ml jacketed reactor described in Example II were added 15.0 grams (0.127 m) alpha-methylstyrene, 15.5 grams (0.1 m) 67.3% t-amyl hydroperoxide and 3.8 grams (0.041 m) phenol. The mixture was stirred to obtain a clear solution and the temperature was adjusted to 20° C. by pumping cool water through the reactor jacket. To this solution was added 1.4 grams (0.009 m) of t-cumyl chloride from the addition funnel over 10 minutes while holding the temperature at 21°-22° C. The reaction was stirred 5 minutes at 22° C., the temperature raised to 25° C. and the reaction stirred 1/2 hour at 30° C., 1/2 hour at 35° C., 11/2 hours at 40° C. and 1/2 hour at 45° C. for a total reaction time of 31/2 hours. At this point essentially all the t-amyl hydroperoxide had been consumed. The reaction was terminated by adding 25 mls of water, stirring 5 minutes, adding 5 mls of 50% NaOH, stirring another 5 minutes and then separating the aqueous caustic layer. The organic layer was washed with saturated NaHCO3 solution, water, 15% NaHSO3, saturated NaHCO3 again and water. The dried material weighed 24.6 grams and contained 54.6% cumyl t-amyl peroxide for a corrected yield of 13.4 grams and a 60.5% yield. The pure cumyl t-amyl peroxide was isolated by fractional distillation under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04241222 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-15114492b7f648d4915bc5c505ed5206 |
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| Source note | uspto-grants-1980_12 |
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