HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924672Generated: October 25, 2026
Iodine → 1-Ethyl-2-iodo-4-(trifluoromethyl)benzene
https://huagongshe.com/reaction/924672
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 4-Ethylbenzotrifluoride | HCID 5324697 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Ethyl-2-iodo-4-(trifluoromethyl)benzene | HCID 70980748 | — |
Reaction Steps
Sulfuric acid (96%, 1.9 mL) was added drop wise to a solution of sodium periodate (3.73 g, 17.4 mmol) and iodine (2.95 g, 11.6 mmol) in a mixture acetic acid (8.45 mL) acetic anhydride (4.23 mL) at 0° C., followed by the drop wise addition of 1-ethyl-4-(trifluoromethyl)benzene (2.0 g, 11.6 mmol). The reaction mixture was let warming up to room temperature while stirring for a period of 24 h. A solution of sodium metabisulfite (10%) was added to quench the remaining iodine and successively, sodium hydroxide (35%) was added to reach pH=7. The aqueous layer was extracted with DCM (3×50 mL) and the combined organic layers were dried over sodium sulfate. Once the solvent was removed, the crude was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09283224B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-9f2fc634e6f5487780f4a0da3f49a8f7 |
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| Source note | uspto-grants-2016_03 |
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