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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993840Generated: October 30, 2026

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

https://huagongshe.com/reaction/1993840

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-(4-imidazol-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 numberUS07652054B2
Source datasetuspto-grants-2010_01
ORD IDord-4ec81581c941495c8643a85ff2afee5d
Source noteuspto-grants-2010_01