참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Monobenzone | HCID 7638 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (R)-tert-Butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylate | HCID 11760051 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(4-Benzyloxy-phenoxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 59753024 | 55.6% |
반응 단계
To a 15 mL of anhydrous DMF was added NaH (60% dispersion in oil, 338 mg, 8.44 mmol), and the resulting reaction mixture was cooled to 0° C. p-benzyloxy phenol (1.41 g, 7.03 mmol) was added and the reaction mixture was stirred at rt for 45 min. It was then cooled to −5° C., and (R)-Boc-prolinol tosylate (2.5 g, 7.03 mmol) in anhydrous DMF (5 mL) was cooled in a separate ice-bath and added dropwise to the reaction mixture. It was then allowed to warm to rt and stirred at 92° C. for 5 h and at rt overnight. The resulting mixture was poured into 200 mL ice/water and stirred for an hour. The resulting precipitate was filtered, washed with ether, dried over MgSO4, concentrated, recrystallized with ether/hexane to give shiny yellow crystals (1.5 g, 55%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728032B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-188a746988c84b5d953e1fe0403ef6ff |
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| 출처 메모 | uspto-grants-2010_06 |
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