참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclopentadiene | HCID 6492 | — |
| 반응물 | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| 반응물 | Trimethylamine oxide dihydrate | HCID 198430 | — |
| 반응물 | Sodium Bisulfite | HCID 23665763 | — |
| 촉매 | Osmium Tetroxide | HCID 30318 | — |
| 촉매 | Tetrabutylammonium Acetate | HCID 82707 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diol | HCID 13166976 | 19.6% |
반응 단계
A slurry of tricyclo[5.2.1.02,6]deca-3,8-diene (26.5 g, 0.2 mol), trimethylamine N-oxide dihydrate (22.3 g, 0.2 mol) and osmium tetroxide (2.5 wt % solution in 2-methyl-2-propanol, 2 □l) in dichloromethane (200 ml) was stirred for 18 h. A further portion of osmium tetroxide (2.5 wt % solution in 2-methyl-2-propanol, ca. 2 □l) was added, water (25 ml) and acetone (50 ml) was added and the reaction mixture was stirred for a further 72 h. Pyridine (0.5 ml) and tetrabutylammonium acetate (0.5 g) were added. Florisil (10 g) and aqueous sodium hydrogensulfite solution was added and the reaction mixture was stirred for 20 min. The reaction mixture was filtered and the product was extracted with dichloromethane (3 times). The combined organic extracts were washed with water, brine and then concentrated to give an oil. The crude oil was purified by flash chromatography eluting with ethyl acetate:hexane (10:90) and then ethyl acetate, to give a waxy solid (6.5 g, 19%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07494992B2 |
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| 출처 데이터셋 | uspto-grants-2009_02 |
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| ORD ID | ord-73906d6b0952423691dcef7cb06941fe |
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| 출처 메모 | uspto-grants-2009_02 |
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