Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6725생성일: 2026년 10월 25일
(4-Phenyl-but-3-ynyl)-carbamic acid tert-butyl ester → cis-4-Phenyl-but-3-enylamine
https://huagongshe.com/reaction/6725
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (4-Phenyl-but-3-ynyl)-carbamic acid tert-butyl ester | HCID 23544319 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | cis-4-Phenyl-but-3-enylamine | HCID 12594566 | — |
반응 단계
A suspension of palladium on barium sulfate (15 mg) was stirred for 15 min in 1 mL pyridine. (4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester (66 mg) was added and the solution was purged with hydrogen then stirred for 1 h under a hydrogen-filled balloon. The solution was diluted with ethyl acetate (10 ml) and washed 3 times with 1 N hydrochloric acid (10 ml). The ethyl acetate layer was dried over sodium sulfate and filtered. The filtrate was evaporated and the resulting residue (54 mg) is primarily cis-(4-phenyl-but-3-enyl)-carbamic acid tert-butyl ester along with (4-phenyl-but-3-ynyl)-carbamic acid tert-butyl ester, 4-phenylbutylamine, and trans-(4-phenyl-but-3-enyl)-carbamic acid tert-butyl ester. The combined minor products constitute ˜20% of the crude material. The tert-butoxycarbonyl group of the desired product was removed by Procedure P to give cis-4-phenyl-but-3-enylamine, which was used in subsequent transformations without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07084154B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-1ba07cbda9804effb51403d0992a3d41 |
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| 출처 메모 | uspto-grants-2006_08 |
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