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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Hexenoic acid, (2E)-HCID 5282707—
반응물1-[4-(5-Hydroxypyrimidin-2-yl)phenyl]-4-pentylbicyclo[2.2.2]octaneHCID 21257762—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물2-[4-(4-Pentylbicyclo[2.2.2]octyl)phenyl]pyrimidin-5-yl (e)-hex-2-enoateHCID 13172237945%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06187393B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-f5ac0fc0e46847b6b8a50de7c2e2ee59
출처 메모uspto-grants-2001_02