Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dithiaoctanediol → tert-butyl 4-[(2Z)-4-hydroxybut-2-en-1-yl]piperidine-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dithiaoctanediol | HCID 78904 | — |
| 반응물 | Tert-butyl 4-(4-hydroxybut-2-yn-1-yl)piperidine-1-carboxylate | HCID 58128571 | — |
| 촉매 | Lindlars catalyst | HCID 131709914 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | tert-butyl 4-[(2Z)-4-hydroxybut-2-en-1-yl]piperidine-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08343990B2 |
| 출처 데이터셋 | uspto-grants-2013_01 |
| ORD ID | ord-fadd0c66e1094505a2a1d9783361977e |
| 출처 메모 | uspto-grants-2013_01 |