関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Di-tert-butyl peroxide | HCID 8033 | — |
| 反応物 | Cyclohexane | HCID 8078 | — |
| 反応物 | Phenyl acetate | HCID 31229 | — |
| 生成物 | Benzene, (cyclohexyloxy)- | HCID 137492 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09416080B2 |
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| 出典データセット | uspto-grants-2016_08 |
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| ORD ID | ord-4fcaf084be86445296ae50a01f11db1d |
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| 出典メモ | uspto-grants-2016_08 |
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