Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8744생성일: 2026년 10월 23일
1-Pentene, 5-bromo- → Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate
https://huagongshe.com/ko/reaction/8744
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Pentene, 5-bromo- | HCID 70704 | — |
| 반응물 | 1-N-Boc-4-Piperidinecarboxylic acid methyl ester | HCID 392870 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate | HCID 11232181 | 99.2% |
반응 단계
To a solution of potassium bis(trimethylsilyl)amide (30.7 g, 0.15 mol) in tetrahydrofuran (750 mL) at 0° C. was added a solution of methyl 1-(tert-butoxycarbonyl)piperidine-4-carboxylate (25 g, 0.10 mol) from Step A in tetrahydrofuran (250 mL) and the reaction mixture was stirred for 1 h. 5-Bromo-1-pentene (19.4 mL, 0.164 mol) was added and the reaction mixture was allowed to warm to room temperature for 1.5 h. The reaction mixture was then poured into saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the title compound (30.9 g) which was used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091211B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-292d55b0aa854c219dbd269febe9a838 |
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| 출처 메모 | uspto-grants-2006_08 |
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