関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzylamine | HCID 7504 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diol | HCID 13166976 | — |
| 反応物 | Sodium periodate | HCID 23667635 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 9-Benzyl-9-aza-tricyclo[5.3.1.02,6]undec-3-ene | HCID 59837848 | 75.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07494992B2 |
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| 出典データセット | uspto-grants-2009_02 |
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| ORD ID | ord-805e761f161547f8804c376da3734b00 |
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| 出典メモ | uspto-grants-2009_02 |
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