Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727191Generated: October 26, 2026

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

https://huagongshe.com/reaction/1727191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 13166976—
ReactantSodium periodateHCID 23667635—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
Solvent1,4-DioxaneHCID 31275—
Product9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-eneHCID 5983784875.4%

Reaction Steps

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%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-805e761f161547f8804c376da3734b00
Source noteuspto-grants-2009_02