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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37588생성일: 2026년 10월 23일

N,N,N',N'-Tetramethylethylenediamine → (E)-2-cyano-3-(2,2-difluoro-1,3-benzodioxol-4-yl)-2-propenoic acid ethyl ester

https://huagongshe.com/ko/reaction/37588

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물2,2-Difluoro-1,3-benzodioxoleHCID 74103—
반응물2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물(E)-2-cyano-3-(2,2-difluoro-1,3-benzodioxol-4-yl)-2-propenoic acid ethyl esterHCID 67735358—

반응 단계

40.0 g (253 mmol) of 2,2-difluoro-1,3-benzodioxole in 29.5 g (254 mmol) of TMEDA and 35 ml of toluene are metallated analogously to Example 2c) at from -15° to -10° C. with 106.2 g (307 mmol) of n-butyllithium solution (18.5% in toluene). 52.1 g (308 mmol) of ethoxymethylenecyanoacetic acid ethyl ester in 115 ml of toluene are added to the reaction mixture at from -15° to -10° C. over a period of 2 hours. The resulting suspension is poured, after 20 minutes at +10° C., into 350 ml of water, the aqueous phase is separated off and the organic phase is concentrated by evaporation in a vacuum rotary evaporator to yield the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420301
출처 데이터셋uspto-grants-1995_05
ORD IDord-7d92c00c0e584bdda70e88162aee2abd
출처 메모uspto-grants-1995_05