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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358074Generated: October 30, 2026

2,4-Dichlorobenzyl chloride → HCID 13232345, compound

https://huagongshe.com/reaction/358074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantP-ChloroacetophenoneHCID 7467—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 13232345HCID 1323234581.9%

Reaction Steps

118 g of 2,4-dichlorobenzyl chloride were added dropwise to 14.6 g of magnesium turnings in 400 ml of dry diethyl ether at the boiling point. After the reaction was complete, a solution of 77.3 g of 4-chloroacetophenone in 400 ml of dry diethyl ether was added. Thereafter, decomposition was effected with aqueous ammonium chloride solution, the organic phase was separated off, washed neutral, dried over sodium sulfate and evaporated down under reduced pressure, the residue was taken up in 1 liter of toluene and the solution was refluxed with 4 g of 4-methylbenzenesulfonic acid, in a water separator. After dehydration was compelete, the toluene phase was washed with sodium carbonate solution and water and dried over sodium sulfate, the solvent was evaproated off and the residue was recrystallized from methanol to give 107 g (81.9%) of E-1-(2,4-dichlorophenyl)-2-(4-chlorophenyl)-prop-1-ene of melting point 84°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464381
Source datasetuspto-grants-1984_08
ORD IDord-6fcc61761d5b4f8d868a7c800939249a
Source noteuspto-grants-1984_08