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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059792Generated: October 30, 2026

Thionyl Chloride → HCID 68916025, compound

https://huagongshe.com/reaction/2059792

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—
ProductHCID 68916025HCID 6891602584.3%

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 (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 numberUS08278307B2
Source datasetuspto-grants-2012_10
ORD IDord-733aa2675bfc4c1baeeb0688c005e0a7
Source noteuspto-grants-2012_10