참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| 반응물 | tert-Butyl N-cyclopropylcarbamate | HCID 15698228 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-nitroso-N-(tert-butoxycarbonyl)amino-cyclopropane | HCID 57941319 | 106.7% |
반응 단계
Nitrosonium tetrafluoroborate (9.32 g, 79.8 mmol) was added carefully in several portions to a cooled (−30° C.) solution of N-(tert-butoxycarbonyl)cyclopropylamine (9.57 g, 60.9 mmol) and anhydrous pyridine (11.7 mL) in dry acetonitrile (150 mL). The solution was stirred at −30° C. for 30 minutes, and then at 0° C. for 2 hours. Ice water and EtOAc were added and the organic phase was separated and washed quickly with 1N HCl to remove pyridine. The organic phase was washed with 1N NaHCO3 and brine, dried (MgSO4), filtered, and evaporated under high vacuum with a water bath temperature below 40° C. to give N-nitroso-N-(tert-butoxycarbonyl)amino-cyclopropane (12.1 g, quantitative) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728029B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-aab3b91cf6294126a849440ff6925f04 |
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| 출처 메모 | uspto-grants-2010_06 |
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