HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482756Generated: October 26, 2026
Di-tert-butyl peroxide → Benzene, (cyclohexyloxy)-
https://huagongshe.com/reaction/1482756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Phenyl acetate | HCID 31229 | — |
| Product | Benzene, (cyclohexyloxy)- | HCID 137492 | — |
Reaction Steps
Into a pressure vessel phenyl acetate (126 μL, 1 mmol, 1 eq) was added and diluted with cyclohexane (1.080 mL, 10 mmol, 10 eq). To this stirring solution was added 1 mol % of a stock solution of {[Cl2NN]Cu}2(benzene) from the catalyst stock solution described in Example 4 (200 μL=0.01 mmol). After adding of tert-butyl peroxide (220 μL, 1.2 mmol), the pressure vessel was sealed and heated to 90° C. for 24 hr. The catalyst was separated by exposing the mixture to air and filtering through Celite®. After removing cyclohexane under vacuum, the residue was analyzed by 1H NMR and GC/MS to determine the yield and consumption of starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416080B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4fcaf084be86445296ae50a01f11db1d |
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| Source note | uspto-grants-2016_08 |
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