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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166379Generated: November 3, 2026

p-Toluenesulfonic acid monohydrate → 1-(4-Methanesulfonyl-phenyl)-2-thiophen-3-yl-4-trifluoromethyl-1H-imidazole

https://huagongshe.com/reaction/1166379

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 22998113HCID 22998113—
SolventTolueneHCID 1140—
Product1-(4-Methanesulfonyl-phenyl)-2-thiophen-3-yl-4-trifluoromethyl-1H-imidazoleHCID 1061927464%

Reaction Steps

A mixture of the 4,5-dihydro-imidazole of step 2 (1.5 g, 3.8 mmol) and p-toluenesulfonic acid monohydrate (0.30 g, 1.5 mmol) in toluene (250 ml) was heated to reflux for 40 hours. An additional p-toluenesulfonic acid monohydrate (0.15 g, 0.78 mmol) was added. The reaction mixture was heated to reflux for 18 hours. The reaction mixture was cooled and the solvent removed under reduced pressure. The crude mixture (3.5 g) was purified by chromatography on silica gel using ethyl acetate/toluene (55/45) to give pure 3-[1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazol-2-yl]thiophene (0.90 g, 64%) as a white solid: mp 194-197° C. Anal. Calc'd. for C15H11N2S2O2F3: C, 48.38, H, 2.98, N. 7.52, S, 17.22. Found: C, 48.74, H, 2.98, N. 7.56, S, 17.45

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613789B2
Source datasetuspto-grants-2003_09
ORD IDord-00f718970968441990af442f1d319707
Source noteuspto-grants-2003_09