Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74860Erstellt: 25. Oktober 2026

Acrylonitrile → 3-(Cholestan-3-yloxy)propanenitrile

https://huagongshe.com/reaction/74860

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylonitrileHCID 7855—
EduktPotassium HydroxideHCID 14797—
Edukt18-Crown-6HCID 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-olHCID 66603436—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Cholestan-3-yloxy)propanenitrileHCID 6743483080%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828952B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-acd60867f8ae432c9d1b12de2d0c0c94
Quellennotizuspto-grants-2014_09