HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719058Generated: November 2, 2026
Hydrogen Peroxide → 2-Octanol, 1-hydroperoxy-
https://huagongshe.com/reaction/719058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | HCID 10511192 | HCID 10511192 | — |
| Catalyst | Tungsten | HCID 23964 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-Octanol, 1-hydroperoxy- | HCID 10583117 | 42% |
Reaction Steps
To a 50 mL flask equipped with a magnetic stirrer and a refluxing condensing tube were added 300 mg of the tungsten-containing mesoporous silicate prepared in Example 2, 760 mg of 60% by weight aqueous hydrogen peroxide solution, 3 g of tert-butanol and 500 mg of 1-octene, and the mixture was stirred and maintained at an inner temperature of 50° C. for 16 hours to react these materials. To the resulting reaction mixture was added 5 g of methyl tert-butyl ether, and the mixture was stirred, and allowed to stand. The supernatant organic layer was analyzed by LC, and it was found that 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane were produced. When the organic layer was analyzed by GC, 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane were thermally decomposed at an injection inlet, and detected as 1-heptanal. Then, the yield of 1-heptanal was determined by GC analysis (internal standard method), and this was regarded as the yield of 2-hydroperoxy-1-hydroxyoctane and 1-hydroperoxy-2-hydroxyoctane. Yield: 42%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132092B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-91f846d116934ed5ba34016083d90089 |
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| Source note | uspto-grants-2006_11 |
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