Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 635139생성일: 2026년 10월 26일
2-Hexenoic acid, (2E)- → 2-[4-(4-Pentylbicyclo[2.2.2]octyl)phenyl]pyrimidin-5-yl (e)-hex-2-enoate
https://huagongshe.com/reaction/635139
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Hexenoic acid, (2E)- | HCID 5282707 | — |
| 반응물 | 1-[4-(5-Hydroxypyrimidin-2-yl)phenyl]-4-pentylbicyclo[2.2.2]octane | HCID 21257762 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-[4-(4-Pentylbicyclo[2.2.2]octyl)phenyl]pyrimidin-5-yl (e)-hex-2-enoate | HCID 131722379 | 45% |
반응 단계
A solution of N,N-dicyclohexylcarbodiimide (0.22 g, 1.1 mmol) in dichloromethane (10 cm3) is added to a solution of (E)-hex-2-enoic acid (0.10 g, 0.9 mmol), 1-[4-(5-hydroxypyrimidin-2-yl) phenyl]-4-pentylbicyclo[2.2.2]octane (0.25 g, 0.9 mmol), 4-(dimethylamino)pyridine (0.04 g) in dichloromethane (20 cm3), cooled in an ice bath (0° C.) under an atmosphere of nitrogen. The reaction mixture is stirred overnight, filtered to remove precipitated material and the filtrate is evaporated down under reduced pressure. The crude product is purified by column chromatography on silica gel using a 9:1 petroleum ether (40-60° C.)/ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield the desired ester (0.15 g, 45%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06187393B1 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-f5ac0fc0e46847b6b8a50de7c2e2ee59 |
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| 출처 메모 | uspto-grants-2001_02 |
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