HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 2-(Ethyl(1-ethynylcyclohexyl)amino)ethan-1-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Cyclohexanol, 1-ethynyl-, 1-acetate | HCID 78903 | — |
| Edukt | Ethylaminoethanol | HCID 18179409 | — |
| Katalysator | Cuprous chloride | HCID 62652 | — |
| Produkt | 2-(Ethyl(1-ethynylcyclohexyl)amino)ethan-1-ol | HCID 22314189 | — |
Reaktionsschritte
To 1.17 ml (12 mmo) ethylaminoethanol in 8 ml THF were added 29.8 mg (0.3 mmol) CuCl, followed by 1 g (6.02 mmol) 1-ethynylcyclohexyl acetate. The solution was stirred at RT for 3 h, the solvent was removed and the residue dissolved in ether/2M HCl. The phases were separated, and after addition of NaOH (pH11) to the aqueous phase, it was extracted with ether. The ether phase was dried over Na2SO4 and concentrated. Distillation by Kugelrohr yielded 2-[Ethyl-(1-ethynyl-cyclohexyl)-amino]-ethanol as colorless oil, MS: 196 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07173043B2 |
| Quelldatensatz | uspto-grants-2007_02 |
| ORD ID | ord-812a42b562b4483992146eccdf850e9a |
| Quellennotiz | uspto-grants-2007_02 |