돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40479생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/40479

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물1,3-CyclopentanedioneHCID 77466—
반응물HCID 178419342HCID 178419342—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매Hydrochloric AcidHCID 313—
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 4-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 diluted 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 번호US08530388B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-34572c46811e4ecc907e60bca4b397f0
출처 메모uspto-grants-2013_09