HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713936Generated: November 1, 2026
Di-tert-butyl peroxide → HCID 178445808, compound
https://huagongshe.com/reaction/713936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 66926809 | HCID 66926809 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178445808 | HCID 178445808 | — |
Reaction Steps
Di-tert-butyl peroxide (0.186 mL, 1.01 mmol) was added to a suspension of Selenium dioxide (0.252 g, 2.27 mmol) in 1,4-Dioxane (6.0 mL). The mixture was stirred for 30 minutes, then 6-(4-tert-Butyl-cyclohexyloxy)-2-methyl-4-trifluoromethyl-quinoline (0.366 g, 1.00 mmol) was added as a solution in 1,4-Dioxane (2.0 mL). The mixture was sealed and was heated at 50° C. for 20 h. The reaction was filtered through Celite and washed with dioxane. The solvent was evaporated and the residue was purified on silica gel column using 0-20% ethyl acetate in hexanes as eluent. Isolated was (Rf=0.70 in 3:1 hexanes/ethyl acetate) the product (212 mg, 56%). ESI-MS(M+H+): 380.20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09186367B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-f8124ee6c35f46b095acc466f59dc44a |
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| Source note | uspto-grants-2015_11 |
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