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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723307Generated: November 1, 2026

Ammonia → 3-(1,3-Dioxolan-2-yl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1723307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl ChlorideHCID 10538915—
SolventTetrahydrofuranHCID 8028—
Product3-(1,3-Dioxolan-2-yl)thiophene-2-sulfonamideHCID 13881752—

Reaction Steps

To 5 ml of liquified ammonia gas dissolved in 50 ml of tetrahydrofuran was added dropwise with stirring and cooling 12.7 g of 3-(1,3-dioxolan-2-yl)thiophene-2-sulfonyl chloride. After stirring overnight at ambient temperature, the tetrahydrofuran was removed in vacuo, water was added to the residue and the mixture was extracted twice with 75 ml of methylene chloride. After washing the combined methylene chloride extracts with water, drying over magnesium sulfate, filtering off the drying agent and evaporation of the methylene chloride, an oily solid residue was obtained. This was chromatographed through silica gel using 1:1 ethyl acetate-hexanes as eluant (Rf 0.35). Evaporation of the solvent mixture yielded 2.2 g of the desired product, as a waxy solid. Infrared absorption spectra showed peaks at 3360, 3260, 1340 and 1140 cm-1, consistent for a primary sulfonamide. Mass spectrum analysis: calc. 235, found 234 (Mass-1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861366
Source datasetuspto-grants-1989_08
ORD IDord-d46d3d0e6b874a518ba822272222e21a
Source noteuspto-grants-1989_08