돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727191생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1727191

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물Sodium CarbonateHCID 10340—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 13166976—
반응물Sodium periodateHCID 23667635—
용매WaterHCID 962—
용매1,1-DichloroethaneHCID 6365—
용매1,4-DioxaneHCID 31275—
생성물9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-eneHCID 5983784875.4%

반응 단계

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%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07494992B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-805e761f161547f8804c376da3734b00
출처 메모uspto-grants-2009_02