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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Iodo-4-methylbenzoic acid | HCID 621640 | — |
| Reactant | 3-(1H-Imidazol-1-YL)-5-(trifluoromethyl)aniline | HCID 44222637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-iodo-4-methylbenzamide | HCID 44222638 | 84.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08778942B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-db391a65307e40be986d6c96c939d646 |
|---|
| Source note | uspto-grants-2014_07 |
|---|