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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418097Generated: November 1, 2026

Ethylene Glycol → 2-(3-Bromothiophen-2-yl)-1,3-dioxolane

https://huagongshe.com/reaction/1418097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTolueneHCID 1140—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-Bromothiophene-2-carboxaldehydeHCID 2797079—
SolventDichloromethaneHCID 6344—
Product2-(3-Bromothiophen-2-yl)-1,3-dioxolaneHCID 12220211—

Reaction Steps

3-bromo-2-formylthiophene (3.89 parts, 0.02M) was heated at reflux with dry ethyleneglycol (1.6 parts) toluene (25 parts) and p-toluene sulphonic acid (0.1 parts) in a vessel equipped with a Dean and Stark separator for 16 hours. The reactants were then cooled and evaporated into silica. The silica was formed into a column which was then developed by elution with hexane containing increasing amounts of dichloromethane. The product was obtained from fractions containing 10-60% dichloromethane as a pale straw-coloured oil (4.42 parts).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880188
Source datasetuspto-grants-1999_03
ORD IDord-9a42a9db6fe040e7a8af27860342855a
Source noteuspto-grants-1999_03