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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl peroxideHCID 8033—
ReactantSelenium DioxideHCID 24007—
ReactantHCID 178422868HCID 178422868—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178445807HCID 17844580720%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340527B2
Source datasetuspto-grants-2016_05
ORD IDord-38fa35853a63461985a318089af100a0
Source noteuspto-grants-2016_05