참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Trimethylsilyl iodide | HCID 85247 | — |
| 반응물 | Ethyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate | HCID 401882 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 8-Azabicyclo(3.2.1)octan-3-one | HCID 434453 | 44.2% |
반응 단계
To a stirred solution of ethyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (500 mg, 2.53 mmol) in 1,2-dichloroethane (10 mL) was added 369 μL (2.60 mmol) of trimethylsilyl iodide (TMSI) under a nitrogen atmosphere. The reaction mixture was heated at 60° C. for 4 h and cooled to room temperature. Methanol (10 mL) was added and the mixture was stirred for 30 min at room temperature (rt). The solvent was removed on vacuo and the residue was partitioned between CH2Cl2 and 1M aqueous NaOH solution (5 mL). The mixture was extracted with CH2Cl2 (3×10 mL). The organic layers were dried over anhydrous Na2SO4, filtered and concentrated under vacuum. The crude material was purified by flash chromatography (silica gel, methylene chloride/EtOH/NEt3 85/10/5) to afford a pale yellow oil (140 mg, 44%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637496B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-b8f9395ae15c4e18b9197e3870cde752 |
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| 출처 메모 | uspto-grants-2014_01 |
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