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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl peroxideHCID 8033—
ReactantSelenium DioxideHCID 24007—
ReactantHCID 66926809HCID 66926809—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178445808HCID 178445808—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-f8124ee6c35f46b095acc466f59dc44a
Source noteuspto-grants-2015_11