Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41072생성일: 2026년 10월 26일
(S)-tert-butyl 3-((R)-2-(pent-4-enoyloxy)-2-phenylethylcarbamoyl)hex-5-enoate → tert-Butyl 2-[(2R,6S,E)-5,12-Dioxo-2-phenyl-1-oxa-4-azacyclododec-8-en-6-yl]acetate
https://huagongshe.com/reaction/41072
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (S)-tert-butyl 3-((R)-2-(pent-4-enoyloxy)-2-phenylethylcarbamoyl)hex-5-enoate | HCID 67310751 | — |
| 촉매 | HCID 178425456 | HCID 178425456 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | tert-Butyl 2-[(2R,6S,E)-5,12-Dioxo-2-phenyl-1-oxa-4-azacyclododec-8-en-6-yl]acetate | HCID 58348121 | 73.1% |
반응 단계
To a solution of (S)-tert-butyl 3-((R)-2-(pent-4-enoyloxy)-2-phenylethylcarbamoyl)hex-5-enoate (470 mg, 1.13 mmol) in toluene (113 mL) was added Grubbs 2nd Generation catalyst (96 mg, 0.113 mmol) and the reaction mixture was heated to 65° C. Upon stirring 7 h with continued heating, TLC analysis indicated complete consumption of starting material. The reaction mixture was cooled to rt, diluted with degassed CH2Cl2 (11 ml) and Pb(OAc)4 (251 mg, 0.566 mmol) was added. The resulting mixture was stirred for 12 h at which point the mixture was passed through a short plug of silica then concentrated using rotary evaporation. The resulting purple solid was triturated with methanol to further remove ruthenium complexes. The off white solid that remained was purified using silica gel chromatography (MeOH/CH2Cl2 gradient) to yield 320 mg of desired product as a white solid in 73% yield. LRMS (M+Na)+: 410.4.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530456B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-50a922f66a094ce8839cea4ea75ace99 |
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| 출처 메모 | uspto-grants-2013_09 |
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