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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622503Generated: October 30, 2026

Thionyl Chloride → N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamide

https://huagongshe.com/reaction/1622503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Iodo-4-methylbenzoic acidHCID 621640—
Reactant3-(1H-Imidazol-1-YL)-5-(trifluoromethyl)anilineHCID 44222637—
SolventDichloromethaneHCID 6344—
ProductN-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamideHCID 4422263884.3%

Reaction Steps

To 3-Iodo-4-methylbenzoic acid (3.07 g, 0.0117 mol) was added thionyl chloride (10 mL) and refluxed for 2 h. The excess thionyl chloride was carefully removed and the resulting acid chloride was dried in vacuo for 2 h. The residue was then dissolved in DCM (anhydrous, 25 mL) and cooled on ice. To the cooled solution was added 3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline 5 (3.46 g, 0.0152 mol) in DCM followed by the dropwise addition of diisopropylethylamine (8.2 mL, 0.047 mol). This was stirred at ambient temperature for 21 h. The white solid that separated was filtered and washed with water and dried to provide 4.65 g of product. Additional product could be obtained from the filtrate following concentration and purification by silica gel flash chromatography in EtOAc/hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778942B2
Source datasetuspto-grants-2014_07
ORD IDord-db391a65307e40be986d6c96c939d646
Source noteuspto-grants-2014_07