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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1798797생성일: 2026년 10월 27일

Dithiaoctanediol → tert-butyl 4-[(2Z)-4-hydroxybut-2-en-1-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1798797

반응식

참여 물질

역할이름HCID투입량
반응물DithiaoctanediolHCID 78904—
반응물Tert-butyl 4-(4-hydroxybut-2-yn-1-yl)piperidine-1-carboxylateHCID 58128571—
촉매Lindlars catalystHCID 131709914—
용매MethanolHCID 887—
생성물tert-butyl 4-[(2Z)-4-hydroxybut-2-en-1-yl]piperidine-1-carboxylateHCID 58128496—

반응 단계

tert-Butyl 4-(4-hydroxybut-2-yn-1-yl)piperidine-1-carboxylate from step 2 of this example (10.6 g, 41.8 mmol) was dissolved in 200 mL MeOH and 3,6-Dithia-1,8-octanediol (191 mg, 1.05 mmol) was added, followed by Lindlar's catalyst (5% w/w, 4.45 g, 2.1 mmol). The reaction vessel was degassed and back filled with hydrogen 3 times and further stirred under a hydrogen balloon at room temperature for 1 hour. The reaction was filtered through Celite and concentrated under vacuum to afford the crude product as colorless oil which was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08343990B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-fadd0c66e1094505a2a1d9783361977e
출처 메모uspto-grants-2013_01