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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6717생성일: 2026년 10월 23일

Water → cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide

https://huagongshe.com/ko/reaction/6717

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-ChlorobenzaldehydeHCID 11477—
반응물(3-(1,3-Dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromideHCID 22018487—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimideHCID 5867982664.3%

반응 조건

온도-78 °C

반응 단계

A mixture of 3-phthalimidopropyltriphenylphosphonium bromide (15.1 g) and 3-chlorobenzaldehyde (4.0 g, Aldrich, U.S.A.) in tetrahydrofuran (150 mL) was cooled to −78° C. in a dry ice/acetone bath. Potassium tert-butoxide (3.2 g) was added and the mixture was stirred for 20 min, then allowed to warm to 0° C. After four hours, the solution was poured into 200 mL water and extracted three times with ethyl acetate. The combined ethyl acetate layers were dried over sodium sulfate, and reduced in vacuo. The residue was dissolved in 200 mL of a 1:1 mixture of ethyl acetate/hexanes, and filtered through a short silica gel plug to remove the triphenylphosphine oxide byproduct. Evaporation of the filtrate yielded 5.7 g of cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide in a 10:1 ratio of cis:trans isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084154B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-789a855a27f04393a01aa7155bdee404
출처 메모uspto-grants-2006_08