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HRID 645333Erstellt: 24. Oktober 2026
Hydrochloric Acid → 2,3,8a-trimethyl-3,4,4a,5,8,8a-hexahydro-1(2H)-naphthalenone
https://huagongshe.com/de/reaction/645333
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | Ethylaluminum dichloride | HCID 11237 | — |
| Edukt | 2-Cyclohexen-1-one, 2,5,6-trimethyl- | HCID 89264 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,3,8a-trimethyl-3,4,4a,5,8,8a-hexahydro-1(2H)-naphthalenone | HCID 57429441 | — |
Reaktionsschritte
In a 1 liter round-bottomed flask, at room temperature, were successively added CH2Cl2 (400 ml), BHT (100 mg) and a 1 M solution of EtAlCl2 in hexanes (80 ml; 0.08 mol). 2,5,6-trimethylcyclohex-2-en-1-one (55.2 g, 0.4 mol, 3:2 mixture of two isomers) was added dropwise, while maintaining the internal temperature below 30° C. Then butadiene (43.2 g, 0.8 mol) was added in one portion. The reaction was stirred at room temperature for 15 days. The reaction was then poured onto cold 5% aqueous HCl and extracted twice with ether. The organic layers were washed with saturated aqueous NaHCO3, water and brine and dried over solid sodium sulfate. The crude product was distilled to give 50 g of a liquid which was then chromatographed on silicagel (heptane:ethyl acetate 49:1) then purified by bulb-to-bulb distillation (B.P.=90° C./0.021 mbar) to give the totle compound (39.43 g, 0.205 mol, 51%) as a 3:2 mixture of diastereoisomers.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07704933B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-579305bd9e9742e297fe5c0214d13473 |
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| Quellennotiz | uspto-grants-2010_04 |
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