Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Quinone | HCID 4650 | — |
| Edukt | 1,3-Cyclohexadiene | HCID 11605 | — |
| Edukt | Lithium acetate | HCID 3474584 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Produkt | 2-Cyclohexene-1,4-diyl Diacetate | HCID 12696435 | 33% |
Reaktionsschritte
Lit., J. Org. Chem., 49:4619 (1984). To a stirred solution of 2.8 g (12.5 mmol) palladium acetate, 27.2 g (267 mmol) lithium acetate, and 7.64 g (70.7 mmol) benzoquinone in 200 ml acetic acid at room temperature were added 26.1 g (300 mmol) manganese dioxide and a solution of 23.8 ml (250 mmol) 1,3-cyclohexadiene in 400 ml pentane, and stirring continued for 16 h. The two-phase reaction mixture was separated and the acetic acid phase extracted twice with pentane. The combined organic extracts were washed successively with saturated brine, water, and 2 M sodium hydroxide solution, then the organic phases were dried over sodium sulphate and concentrated in vacuo. Recrystallisation from pentane afforded 16.1 g (33%) of the title compound as an off-white crystalline solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06103910 |
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| Quelldatensatz | uspto-grants-2000_08 |
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| ORD ID | ord-5f4921574a0840c6bcdfbb1e531c8dcd |
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| Quellennotiz | uspto-grants-2000_08 |
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