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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231104Generated: November 1, 2026

Methanol → 4-(3-fluoro-4-methoxyphenyl)-5-[4-(methylsulfonyl)phenyl]-2-(trifluoromethyl)-1H-imidazole

https://huagongshe.com/reaction/2231104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 178489083HCID 178489083—
SolventWaterHCID 962—
Product4-(3-fluoro-4-methoxyphenyl)-5-[4-(methylsulfonyl)phenyl]-2-(trifluoromethyl)-1H-imidazoleHCID 18463536—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(3-Fluoro-4-methoxyphenyl)-5-[4-(methylthio)phenyl]-2-(trifluoromethyl)-1H-imidazole (516 mg, 1.35 mmol) from step 4 was dissolved in methanol (10 ml) and cooled to 0° C. OXONE® (2.46 g, 4 mmol) in water (10 ml) was added. After the addition, the ice bath was removed and the reaction was stirred at ambient temperature for 3 hours. The mixture was extracted with chloroform (3×50 ml). The combined organic phases were dried (MgSO4) and concentrated in vacuo. The residue was purified by chromatography, affording 4-(3-fluoro-4-methoxyphenyl)-5-[4-(methylsulfonyl)phenyl]-2-(trifluoromethyl)-1H-imidazole as a solid (98 mg): m.p. 228-234° C. (DSC) The structure assignment was supported by NMR. Mass spectrum (EI, m/e): 414. Anal. Calc'd. for C18H14N2F4O3S: C, 52.17; H, 3.41; N, 6.76. Found: C, 52.30; H, 3.62; N, 6.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426360B1
Source datasetuspto-grants-2002_07
ORD IDord-856a9dfabd2e4b3ca7e137102e5337d8
Source noteuspto-grants-2002_07