HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043491Generated: October 26, 2026
Potassium Iodide → 1,3-Dichloro-2-iodo-5-(trifluoromethoxy)benzene
https://huagongshe.com/reaction/1043491
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,6-Dichloro-4-(trifluoromethoxy)aniline | HCID 688247 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dichloro-2-iodo-5-(trifluoromethoxy)benzene | HCID 66886425 | — |
Reaction Steps
2,6-Dichloro-4-(trifluoromethoxy)aniline (4.65 g, 13.2 mmol) suspended in 1 M of HCl solution (100 mL) was treated at 0° C. with sodium nitrite (0.913 g, 13.2 mmol) in water dropwise. After 15 minutes at 0° C., potassium iodide (2.20 g, 13.2 mmol) in water was added and the solution was heated at 40° C. for 15 min. The solution was quenched with saturated aq. Na2S2O3 solution (100 mL), and extracted with ethyl acetate (300 mL). The organic phase was washed with 0.1 N HCl solution satd. aq. NaHCO3 sol. (500 mL), and dried over sodium sulfate. Purification by silica gel chromatography (10-40% EtOAc/hexanes) afforded the desired product as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563541B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a586d1e25e044628b792359eaab2f7b8 |
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| Source note | uspto-grants-2013_10 |
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