HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471458Generated: November 3, 2026
Iodine → 2-Bromo-1-iodo-3-(trifluoromethyl)benzene
https://huagongshe.com/reaction/471458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 2-Bromo-3-(trifluoromethyl)aniline | HCID 94058 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-1-iodo-3-(trifluoromethyl)benzene | HCID 53484470 | 85.5% |
Reaction Steps
2-Bromo-3-trifluoromethylaniline (8 g, 33.33 mmol) is suspended in water (90 mL) and cooled to 0° C. 96% H2SO4 (26.7 mL, 13.7 mmol) is added and the mixture stirred for 30 minutes. NaNO2 (2.41 g, 35 mmol) is dissolved in a small quantity of water and added dropwise at 0° C. The mixture is stirred for 30 minutes then potassium iodide (9.24 g, 55.66 mmol) and iodine (9.31 g, 36.66 mmol) in water are added dropwise with cooling. The mixture is stirred until gas evolution ceases then warmed to 40° C. and allowed to cool to room temperature. The mixture is shaken with excess aqueous Na2SO3 solution and extracted with ethyl acetate. The organic extracts are evaporated and the residue purified by flash chromatography (eluent: cyclohexane) to give the title compound (Yield 10.0 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08633182B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-a6e6edc46afe4276bf509ccdc0aa1228 |
|---|
| Source note | uspto-grants-2014_01 |
|---|