참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | N-Boc-p-toluenesulfonamide | HCID 688170 | — |
| 반응물 | (E)-2-Pentenal | HCID 5364752 | — |
| 반응물 | (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether | HCID 11198150 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | (2R,3S)-tert-butyl 2-ethyl-3-formylaziridine-1-carboxylate | HCID 90121328 | — |
반응 단계
To a 500 mL round-bottom flask equipped with a stir bar was added (S)-2-(diphenyl((trimethylsilyl)oxy)methyl)pyrrolidine (2.60 g, 8.00 mmol) and CHCl3 (200 mL). To the solution was added tert-butyl tosylcarbamate (10.9 g, 40.0 mmol). The flask was placed in a room temperature-water bath. To the stirred solution was added sodium acetate (9.84 g, 120 mmol), then (E)-pent-2-enal (4.04 g, 48.0 mmol). The mixture was stirred at room temperature for 40 minutes. The mixture was filtered, washing the filter cake with a small amount of CHCl3. The filtrate was concentrated in vacuo at 30° C. The resulting orange liquid was dissolved in Et2O (400 mL) and transfered to a 1 L separatory funnel. The solution was washed with water:aq. sat. NaHCO3 (200 mL:200 mL). The aqueous phase was extracted with Et2O (100 mL). The combined organics were washed with brine (200 mL); dried over MgSO4; filtered; then concentrated in vacuo to afford (2R,3S)-tert-butyl 2-ethyl-3-formylaziridine-1-carboxylate as a pale orange liquid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09334279B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-74e9e9d7f9554b9fa6d24097e1c753d9 |
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| 출처 메모 | uspto-grants-2016_05 |
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