Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Cyanovinyl acetate | HCID 18291 | — |
| Edukt | 2-(Trimethylsiloxy)-1,3-cyclohexadiene | HCID 4095656 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Bicyclo(2.2.2)octane-2,5-dione | HCID 13570060 | — |
Reaktionsschritte
25 mL of 2-(trimethylsilyloxy)-1,3-cyclohexadiene and 13 mL of α-acetoxyacrylonitrile were mixed and heated at 150° C. in a closed vessel for 22 h. The obtained dark orange viscous oil was dissolved in 200 mL of MeOH. After dropwise addition of a solution of 2.2 g of sodium methoxide in 150 mL of MeOH the reaction mixture was stirred for 3 h at rt, poured into ice/water and extracted with DCM. The organic phases were concentrated in vacuo and the crude residue was purified by CC with EtOAc-Hept (1:2) to yield 7.9 g of rac-(1R*,4R*)-bicyclo[2.2.2]octane-2,5-dione.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08202885B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-908da1bc3303458a97e0e63b60158d7b |
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| Quellennotiz | uspto-grants-2012_06 |
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