Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 3-Methoxypropyne | HCID 69393 | — |
| Edukt | Lithium Bromide | HCID 82050 | — |
| Edukt | 4-(Dimethylamino)-4-phenylcyclohexan-1-one | HCID 11424492 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 86634679 | HCID 86634679 | — |
Reaktionsschritte
Methyl propargyl ether (0.36 g, 5.2 mmol) dissolved in abs. THF (5 mL) was added in drops to a 2.5 M solution of butyl lithium in hexane (2.1 mL, 5.2 mmol) at −30° C. in argon. A solution of 4-dimethylamino-4-phenylcyclohexanone (1.08 g, 5.0 mmol) in abs. THF (5 mL) and lithium bromide (0.22 g, 2.5 mmol) dissolved in abs. THF (2.0 mL) was then added at −30° C. The reaction mixture was heated to −5° C., mixed in drops with a solution of benzyl bromide (1.28 g, 7.5 mmol) in abs. DMSO (10 mL) and stirred 2 h at 50° C. For work up of the reaction mixture water (10 mL) was added with ice bath cooling and extracted with cyclohexane (4×20 mL). The organic phase was washed with 20% ammonium chloride solution, dried over Na2SO4 and concentrated to low volume in a vacuum. The remaining residue was purified by flash chromatography with CHCl3/MeOH (40:1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835689B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-a9aa16dfd7fd4cdfac553552dfcd70be |
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| Quellennotiz | uspto-grants-2014_09 |
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