Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Cyclohexanone | HCID 7967 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Cyclohexanone, 2-(2-propen-1-yl)- | HCID 78944 | 71,6% |
Reaktionsschritte
EX-6a) A suspension of potassium t-butoxide (200 g, 1.78 mol) in toluene which was cooled to 0° C. in an ice bath under N2 was treated with cyclohexanone (157 g, 1.60 mol). To the reaction mixture was slowly added allyl bromide (194 g, 1.60 mol) over a 2 hour period. The reaction was warmed to room temperature over 5 hours. The reaction was then poured into EtOAc (400 mL) and washed once with 10% potassium hydrogen sulfate (250 mL). The organic solution was then washed with brine (3×200 mL), dried over magnesium sulfate, and evaporated under reduced pressure. The resulting oil was then chromatographed to yield 158.4 g (71.6%) of 2-allyl cyclohexanone as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06552052B2 |
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| Quelldatensatz | uspto-grants-2003_04 |
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| ORD ID | ord-5b546ca4dfc34bd8948828b7d13c1651 |
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| Quellennotiz | uspto-grants-2003_04 |
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