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HRID 322839作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dichloro-1-iodobenzeneHCID 96864—
反応物Diethyl iodofumarateHCID 5359100—
反応物MagnesiumHCID 5462224—
触媒Ethyl BromideHCID 6332—
触媒ZincchlorideHCID 3007855—
触媒Triphenylphosphine palladium dichlorideHCID 13169693—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物(E)-2-(2,4-dichlorophenyl)-butendioic acid diethyl esterHCID 6997233463%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211387B1
出典データセットuspto-grants-2001_04
ORD IDord-a3223a29b6914e1cbaafc418aa9f31aa
出典メモuspto-grants-2001_04