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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644833Generated: October 30, 2026

Trifluoroacetic acid → 3-(4-Imidazol-1-ylmethylphenyl)-5-butylthiophene-2-sulfonamide

https://huagongshe.com/reaction/1644833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(4-Bromobenzyl)-1H-imidazoleHCID 2989557—
Reactant3-(4-Imidazol-1-ylmethylphenyl)-5-butyl-N-tert-butylthiophene-2-sulfonamideHCID 11994031—
CatalystAnisoleHCID 7519—
Product3-(4-Imidazol-1-ylmethylphenyl)-5-butylthiophene-2-sulfonamideHCID 6677510249%

Reaction Steps

Trifluoroacetic acid was added (10 mL) to the crude 3-(4imidazol-1-ylmethylphenyl)-5-butyl-N-tert-butylthiophene-2-sulfonamide from step (c) above, and one drop (ca. 0.05 mL) of anisol was added to the mixture. The reaction mixture was stirred under N2 atmosphere for 30 hours and then evaporated and co-evaporated with acetonitrile. The crude product was purified by column chromatography (CH2Cl2:MeOH (20:1)) to give sub-title compound (232 mg, 0.62 mmol) in 49% yield (from 1-(4-bromobenzyl)-1H-imidazole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124638B2
Source datasetuspto-grants-2012_02
ORD IDord-bc4b42bdb04d418d9011c63cdec74c33
Source noteuspto-grants-2012_02