HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acrylonitrile → 3-(Cholestan-3-yloxy)propanenitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acrylonitrile | HCID 7855 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Edukt | (6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-1-ol | HCID 66603436 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(Cholestan-3-yloxy)propanenitrile | HCID 67434830 | 80% |
Reaktionsschritte
Cholestanol (1.554 g, 3.998 mmol) was dissolved in DCM (6 mL). To this solution was added KOH (40% w/w in water, 1.2 mL) and acrylonitrile (0.8 mL), followed by 18-crown-6 (104 mg). The mixture was stirred at room temperature overnight. The organic layer was washed with brine and dried (Na2SO4) before the solvent was evaporated. The residue was recrystallized from hot MeOH to yield the pure product as a colourless crystalline solid (1.42 g, 80% yield). 1H NMR (400 MHz, CDCl3) δ: 3.68 (t, 2H, CH2O), 3.29 (m, 1H, CHO), 2.57 (t, 2H, CH2CN), 1.98-0.58 (m, 31H), 0.89 (d, 3H, J=6.6, CH3), 0.87 (d, 3H, J=1.8, CH3), 0.85 (d, 3H, J=2.0, CH3), 0.79 (s, 3H, CH3), 0.64 (s, 3H, CH3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08828952B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-acd60867f8ae432c9d1b12de2d0c0c94 |
| Quellennotiz | uspto-grants-2014_09 |