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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1727191Erstellt: 26. Oktober 2026

Benzylamine → 9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-ene

https://huagongshe.com/reaction/1727191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzylamineHCID 7504—
EduktSodium CarbonateHCID 10340—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 13166976—
EduktSodium periodateHCID 23667635—
LösungsmittelWaterHCID 962—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-eneHCID 5983784875,4%

Reaktionsschritte

To a stirred solution of tricyclo[5.2.1.02,6]dec-3-ene-8,9-diol (Preparation 36, 6.24 g, 37.6 mmol) in dioxane (100 ml) was added sodium periodate (8.04 g, 37.6 mmol) in water (80 ml) and the reaction mixture was stirred vigorously for 45 min. The reaction mixture was extracted with ethyl acetate (4×100 ml) and the combined extracts were washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude oil (6.1 g, 37.1 mmol) was diluted with dichloroethane (400 ml) and benzylamine (3.98 g, 37.1 mmol) was added. After 3 min, sodium triacetoxyborohydride (25.23 g, 119 mmol) was added and the reaction mixture was stirred at room temperature for 18 h. Saturated sodium carbonate solution (200 ml) was added, and after 30 min, the layers were separated and the aqueous layer was washed with dichloromethane (3×50 ml). The combined organic extracts were washed with brine, filtered and concentrated. The crude yellow oil was purified by flash chromatography eluting with ethyl acetate:dichloromethane (10:90) to give the title compound as a colourless oil (6.7 g, 75%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07494992B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-805e761f161547f8804c376da3734b00
Quellennotizuspto-grants-2009_02