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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1413913생성일: 2026년 10월 24일

Ethanone, 2-(2-imidazolidinylidene)-1-phenyl- → 2-(2-Ethoxy-2-phenyl-ethenyl)-2-imidazoline tetrafluoroborate

https://huagongshe.com/ko/reaction/1413913

반응식

참여 물질

역할이름HCID투입량
반응물Ethanone, 2-(2-imidazolidinylidene)-1-phenyl-HCID 821546—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
용매DichloromethaneHCID 6344—
생성물2-(2-Ethoxy-2-phenyl-ethenyl)-2-imidazoline tetrafluoroborateHCID 86736218—

반응 단계

20 g (0.105 mole) of triethyloxonium-tetrafluoroborate is dissolved in 200 ml of methylene chloride. To the solution is added 18.8 g (0.1 mole) of crystalline 2-(2--imidazolidinylidene)-acetophenone [m.p. 211°-212°, see J. Klosa, Arch. Pharmaz. 286, 397 (1953)]. After the slightly exothermic reaction has subsided, the reaction mixture, a clear yellow solution, is stirred for 16 hours at room temperature; it is subsequently concentrated to dryness in the rotary evaporator; and the crystallising residue is suspended in 300 ml of ethyl acetate. The suspension is cooled to 5°, and the crystals are filtered off with suction to obtain 2-(2-ethoxy-2-phenyl-ethenyl)-2-imidazoline-tetrafluoroborate, m.p. 151°-152°. After drying at 60° in vacuo, the product is further employed without additional purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04251542
출처 데이터셋uspto-grants-1981_02
ORD IDord-a56c90f0bd6d488d91215fc73f661ba4
출처 메모uspto-grants-1981_02