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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578433Generated: November 2, 2026

p-Toluenesulfonic acid → 2-(Bromomethyl)-4-[(4-chlorophenoxy)methyl]-2-(4-chlorophenyl)-1,3-dioxolane

https://huagongshe.com/reaction/1578433

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantChlorphenesinHCID 7697—
Reactantp-Chlorophenacyl bromideHCID 68303—
SolventBenzeneHCID 241—
Product2-(Bromomethyl)-4-[(4-chlorophenoxy)methyl]-2-(4-chlorophenyl)-1,3-dioxolaneHCID 20332649—

Reaction Steps

A mixture of 11.7 parts of 2-bromo-4'-chloroacetophenone, 12.2 parts of 1-(p-chlorophenoxy)-2,3-propanediol, 3 parts of p-toluenesulfonic acid and 240 parts of benzene is stirred and refluxed for 20 hours in a four-necked round-bottom flask equipped with a watertrap. The benzene solution is washed successively with a diluted sodium hydroxide solution and with water. The solvent is removed in vacuo. The residue is triturated in methanol. The precipitated product is filtered off (methanol filtrate is set aside) and crystallized from toluene, yielding A-2-(bromomethyl-4-(p-chlorophenoxymethyl)-2-(p-chlorophenyl)-1,3-dioxolane; m.p. 165°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03936470
Source datasetuspto-grants-1976_02
ORD IDord-ed4f67585ce84caeb44a058025c132e3
Source noteuspto-grants-1976_02