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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339476생성일: 2026년 10월 23일

Hydrochloric Acid → 2-(5-Bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione

https://huagongshe.com/ko/reaction/339476

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TolueneHCID 1140—
반응물1,3-CyclopentanedioneHCID 77466—
반응물HCID 178419342HCID 178419342—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물2-(5-Bromo-2-cyclopropylphenyl)cyclopentane-1,3-dioneHCID 66676860—

반응 조건

온도80 °C

반응 단계

To a solution of cyclopentane-1,3-dione (0.57 g, 0.0058 mol) and N,N-dimethylaminopyridine (3.64 g, 0.030 mol) in chloroform (33 ml) is added toluene (9 ml) then 5-bromo-2-cyclopropylphenyl lead triacetate (3.77 g, 0.0065 mol). This solution is heated at 80° C. for 20 hours then cooled to room temperature and dilluted with dichloromethane and 2M aqueous hydrochloric acid. The resulting biphasic suspension is filtered through diatomaceous earth and the two phases are separated. The organic layer is further washed with 2M aqueous hydrochloric acid and the aqueous phase is extracted again with dichloromethane. All organic fractions are combined, washed with brine, dried over magnesium sulfate then concentrated in vacuo. The crude product is finally purified by flash column chromatography on silica gel (isohexane/ethyl acetate eluant) to afford 2-(5-bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895474B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-551c3ce23a114421a780d304ee390544
출처 메모uspto-grants-2014_11