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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322839생성일: 2026년 10월 24일

2,4-Dichloro-1-iodobenzene → (E)-2-(2,4-dichlorophenyl)-butendioic acid diethyl ester

https://huagongshe.com/ko/reaction/322839

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-1-iodobenzeneHCID 96864—
반응물Diethyl iodofumarateHCID 5359100—
반응물MagnesiumHCID 5462224—
촉매Ethyl BromideHCID 6332—
촉매ZincchlorideHCID 3007855—
촉매Triphenylphosphine palladium dichlorideHCID 13169693—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물(E)-2-(2,4-dichlorophenyl)-butendioic acid diethyl esterHCID 6997233463%

반응 조건

온도0 °C

반응 단계

A suspension of magnesium (0.73 g, 0.03 moles) in ethyl ether (20 ml) under nitrogen flow was added with ethyl bromide (50 mg). The solution was stirred for 15 minutes then added with a solution of 1,3-dichloro-4-iodobenzene (5.45 g, 0.02 moles) in ethyl ether (10 ml) in 1 hour keeping the temperature at 18-22° C. At the end of the addition the suspension was kept under stirring for 90 minutes at 18-22° C., then decanted and the surnatant added in 10 minutes to a suspension of dry zinc chloride (5.4 g, 0.04 moles) in ethyl ether (8 ml). At the end of the addition the stirring was kept on at 20° C. for further 90 minutes, then cooled to 0° C. DMF (10 ml) and palladium dichloride triphenylphosphine (351 mg, 0.0005 moles), then a solution of diethyl iodo-fumarate (4.18 g, 0.014 moles) in DMF (4 ml) were added. The mixture was kept under stirring for 15 hours at 25° C. and after a work-up similar to the one of point a) 2.1 g of (E)-2-(2,4-dichlorophenyl)-butendioic acid diethyl ester were yielded (yield: 63% calculated with respect to the iodo-furmarate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211387B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-a3223a29b6914e1cbaafc418aa9f31aa
출처 메모uspto-grants-2001_04