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HRID 1727191作成日:2026年10月27日

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

https://huagongshe.com/reaction/1727191

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物Sodium CarbonateHCID 10340—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 13166976—
反応物Sodium periodateHCID 23667635—
溶媒WaterHCID 962—
溶媒1,1-DichloroethaneHCID 6365—
溶媒1,4-DioxaneHCID 31275—
生成物9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-eneHCID 5983784875.4%

反応手順

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%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07494992B2
出典データセットuspto-grants-2009_02
ORD IDord-805e761f161547f8804c376da3734b00
出典メモuspto-grants-2009_02