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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719058Generated: November 2, 2026

Hydrogen Peroxide → 2-Octanol, 1-hydroperoxy-

https://huagongshe.com/reaction/719058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactanttert-ButanolHCID 6386—
Reactant1-OcteneHCID 8125—
ReactantHCID 10511192HCID 10511192—
CatalystTungstenHCID 23964—
Solventtert-Butyl methyl etherHCID 15413—
Product2-Octanol, 1-hydroperoxy-HCID 1058311742%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132092B2
Source datasetuspto-grants-2006_11
ORD IDord-91f846d116934ed5ba34016083d90089
Source noteuspto-grants-2006_11