HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422609Generated: November 1, 2026
Iodine → 2-Bromo-1-iodo-3-(trifluoromethyl)benzene
https://huagongshe.com/reaction/1422609
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| 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 | — |
Reaction Steps
An ice-cold solution of NaNO2 (0.15 g) in water (0.5 mL) is added to a mixture of 2-bromo-3-trifluoromethyl-aniline (0.48 g), concentrated H2SO4 (2 mL), and water (1.8 mL) at ca. 5° C. The mixture is stirred in the cooling bath for 20 min and then poured into a solution of KI (0.56 g) and I2 (0.56 g) in water (0.5 mL). After gas evolution ceases, the mixture is heated to 40° C. and stirred at this temperature for 1 h. The mixture is cooled to room temperature and aqueous Na2SO3 solution is added. The resulting mixture is extracted with ethyl acetate, and the combined extracts are dried (Na2SO4) and concentrated. The solvent is evaporated and the residue is chromatographed (cyclohexane/ethyl acetate 95:5→90:10) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927531B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-381a02c6b88d4df79d9454cce2a87247 |
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| Source note | uspto-grants-2015_01 |
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