HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525439Generated: October 29, 2026
Di-tert-butyl peroxide → HCID 178445807, compound
https://huagongshe.com/reaction/525439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 178422868 | HCID 178422868 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178445807 | HCID 178445807 | 20% |
Reaction Steps
Di-tert-butyl peroxide (1.93 mL, 10.5 mmol) was added to a suspension of selenium dioxide (2.68 g, 24.1 mmol) in 1,4-dioxane (24.00 mL, 307.5 mmol). The mixture was stirred for 30 minutes, then 6-(trans-4-tert-Butyl-cyclohexyloxy)-2-methylquinoline (3.12 g, 10.5 mmol) was added as a solution in 1,4-Dioxane and the mixture was heated overnight at 50° C. The reaction mixture was then cooled to room temperature, diluted in chloroform and filtered through a pad of celite. The filtrate was washed with water. The layers were separated and the combined organic phase was dried over MgSO4, filtered, concentrated under reduced pressure, adsorbed onto silica gel and purified by flash chromatography (0-30% EtOAc in hexanes) to give the title compound as a pale yellow solid in 20% yield. ESI-MS (M+H+): 312.27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340527B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-38fa35853a63461985a318089af100a0 |
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| Source note | uspto-grants-2016_05 |
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