Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75147Erstellt: 23. Oktober 2026

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol

https://huagongshe.com/de/reaction/75147

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
Edukt2-[4-(Benzyloxy)phenyl]oxiraneHCID 13248717—
LösungsmittelIsopropanolHCID 3776—
Produkt1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanolHCID 5943717623,2%

Reaktionsschritte

2-(4-(benzyloxy)phenyl)oxirane (2 g, 8.8 mmol) and (1-adamantylmethyl)amine (1.46 g, 8.8 mol) were dissolved in isopropyl alcohol (30 mL) and heated under reflux overnight. The mixture was concentrated to give the crude product, which was purified by column chromatography to afford 1-(4-(benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol (0.8 g, 23%). 1H NMR: (CDCl3, 400 MHz) δ=1.51 (m, 6H), 1.60-1.72 (m, 6H), 1.97 (m, 3H), 2.32&2.45 (dd, 2H), 2.64 (m, 1H), 2.73 (m, 1H), 2.94 (m, 1H), 3.40 (brs, 3H), 4.79 (m, 1H), 6.93 (m, 2H), 7.26-7.43 (m, 7H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835426B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-88047b6c7522438b9fa11d82686d0f95
Quellennotizuspto-grants-2014_09