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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444597Generated: October 27, 2026

Water → Thiophene-2-sulfonyl bromide

https://huagongshe.com/reaction/444597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantBromineHCID 24408—
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
ReactantThiophene-2-sulfonohydrazideHCID 2064119—
ProductThiophene-2-sulfonyl bromideHCID 12874989—

Reaction Conditions

Temperature15 °C

Reaction Steps

In the reaction, excess hydrazine in the presence of a solvent, advantageously a lower alkanol, is reacted with the 2-thiophenesulfonyl chloride to form a 2-thiophenesulfonyl hydrazine. In the reaction, the 2-thiophenesulfonyl chloride is gradually added to the hydrazine solution which is maintained at a low temperature, advantageously between about 5° and up to about 15° C. The reaction mixture is then allowed to warm to room temperature, the solvent is removed in vacuo and a mixture of a heavy oil and a fluffy solid results. This mixture is treated with water and the solid is dissolved and the oil separated therefrom. This mixture of oil and water, which contains the hydrazine hydrochloride from the first reaction, is then placed in a flask containing a bromine solvent, advantageously chloroform, crushed ice is added thereto and to the resulting slurry bromine is added at such a rate that the reaction temperature remains below about 10° C. After the bromine has been added and the bromine color has dissipated, the layers are separated, the chloroform layer is dried over an appropriate desiccant, advantageously anhydrous magnesium sulfate, and the chloroform removed in vacuo to leave a yellow oil which crystallizes on addition of hexane to give the 2-thiophenesulfonyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264774
Source datasetuspto-grants-1981_04
ORD IDord-e6a43b27644f43efa6c48fdfeb531030
Source noteuspto-grants-1981_04