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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081757Generated: November 2, 2026

Benzene → 2-(3-Thienyl)-1,3-dioxolane

https://huagongshe.com/reaction/2081757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-ThiophenecarboxaldehydeHCID 68135—
Product2-(3-Thienyl)-1,3-dioxolaneHCID 31563072%

Reaction Steps

In a 100 mL roundbottom flask equipped with a dean stark trap and a reflux condenser, thiophene-3-carboxaldehyde and 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 (93°-95° C., 7.5 mm Hg) afforded 45.3 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-f16eb09f4e884bef94b79530b38c41c9
Source noteuspto-grants-1993_02