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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081756Generated: November 1, 2026

Benzene → 2-(4-Bromothiophen-2-yl)-1,3-dioxolane

https://huagongshe.com/reaction/2081756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
Product2-(4-Bromothiophen-2-yl)-1,3-dioxolaneHCID 385725572%

Reaction Steps

In a 100 mL roundbottom flask equipped with a dean stark trap and a reflux condenser, 4-bromothiophene-2-carboxaldehyde (25 g, 131 mMol) and a catalytic amount of p-toluenesulfonic acid were dissolved in benzene (50 mL). The mixture was heated to reflux overnight. The reaction was cooled, washed with sat'd sodium bicarbonate, water, dried (MgSO4) and concentrated. Purification by fractional distillation (80°-90° C., 0.5 mm Hg) afforded 24.23 g (72%) of the desired dioxolane as a clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185363
Source datasetuspto-grants-1993_02
ORD IDord-410fc2c968474776b0367118b95eccbe
Source noteuspto-grants-1993_02