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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322839Generated: October 25, 2026

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

https://huagongshe.com/reaction/322839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-1-iodobenzeneHCID 96864—
ReactantDiethyl iodofumarateHCID 5359100—
ReactantMagnesiumHCID 5462224—
CatalystEthyl BromideHCID 6332—
CatalystZincchlorideHCID 3007855—
CatalystTriphenylphosphine palladium dichlorideHCID 13169693—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product(E)-2-(2,4-dichlorophenyl)-butendioic acid diethyl esterHCID 6997233463%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211387B1
Source datasetuspto-grants-2001_04
ORD IDord-a3223a29b6914e1cbaafc418aa9f31aa
Source noteuspto-grants-2001_04