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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

반응식

참여 물질

역할이름HCID투입량
반응물1-Pentene, 5-bromo-HCID 70704—
반응물1-N-Boc-4-Piperidinecarboxylic acid methyl esterHCID 392870—
반응물Sodium BicarbonateHCID 516892—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylateHCID 1123218199.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-292d55b0aa854c219dbd269febe9a838
출처 메모uspto-grants-2006_08