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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706876Generated: October 30, 2026

Benzene → 2-(Bromomethyl)-2,4-bis(4-chlorophenyl)-1,3-dioxolane

https://huagongshe.com/reaction/1706876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-Chlorophenacyl bromideHCID 68303—
Reactant1-(4-Chlorophenyl)-1,2-ethanediolHCID 101107—
SolventWaterHCID 962—
Product2-(Bromomethyl)-2,4-bis(4-chlorophenyl)-1,3-dioxolaneHCID 20332620—

Reaction Steps

A mixture of 11.7 parts of 2-bromo-4'-chloroacetophenone, 9 parts of 1-(p-chlorophenyl)-1,2-ethanediol, 0.5 parts of p-toluenesulfonic acid and 80 parts of benzene is stirred and refluxed for 2 days with water-separator. The reaction mixture is cooled and washed successively twice with a sodium hydrogen carbonate solution and once with water. The organic phase is dried and evaporated. The residue is triturated in petroleum ether and cooled on ice. The precipitated product is filtered off, crystallized from methanol, stirred in acetonitrile while cooling on ice, filtered off again and washed once more with acetonitrile, yielding 2-(bromomethyl)-2,4-bis(p-chlorophenyl)-1,3-dioxolane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209447
Source datasetuspto-grants-1980_06
ORD IDord-700a3e22731848aeb67d8cb1901608bf
Source noteuspto-grants-1980_06