Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanethiol | HCID 6343 | — |
| Edukt | Bromomethyl tricyclo[3.3.1.13,7]dec-1-yl ketone | HCID 197820 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Adamantyl (Ethylthio)methyl Ketone | HCID 53882109 | — |
Reaktionsschritte
Ethyl mercaptan (5.76 ml., 4.83 g., 0.078 mol) in 250 ml. THF was cooled to -70°. n-Butyllithium (50 ml. of 1.55M in hexane, 0.078 mol) was added over 10 minutes at that temperature. The mixture was then allowed to warm to 10°, recooled to -70°, and 1-adamantyl bromomethyl ketone (20 g., 0.078 mol) in 125 ml. THF added over. The mixture was stirred 15 minutes at -70° C., stripped to one fifth volume, diluted to 600 ml. with ether, washed 2×200 ml. saturated NH4Cl, 3×150 ml. H2O and 1×200 ml. brine, dried over MgSO4 and stripped to yield title product as an oil, 18.5 g. 1H-nmr (300 MHz) 1.2 (t, 3H), 1.6-2.1 (m, 15H), 2.5 (q, 2H), 3.35 (s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04762921 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-34f01fc627254bcf8470d76189645de3 |
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| Quellennotiz | uspto-grants-1988_08 |
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