HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62760Generated: October 30, 2026
Iodine → 2-Chloro-5-iodo-1,3-dimethoxybenzene
https://huagongshe.com/reaction/62760
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-Chloro-3,5-dimethoxybenzenamine | HCID 67041835 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-5-iodo-1,3-dimethoxybenzene | HCID 67041737 | 68.1% |
Reaction Steps
4-Chloro-3,5-dimethoxyaniline (2) (6.61 g, 35.2 mmol) was added to a mixture of sulfuric acid (9.39 mL, 176 mmol) and H2O (100 mL) at 00° C. Sodium nitrite (3.16 g, 45.8 mmol) was added and the reaction mixture was stirred at 0° C. for 30 min. The mixture was added to a pre-warmed mixture of sodium iodide (21.1 g, 141 mmol), iodine (4.47 g, 17.6 mmol), sulphuric acid (8 mL) and H2O (100 mL) at 80° C. and the resulting mixture was heated at reflux for 30 min. The mixture was allowed to cool to RT and then 40% sodium thiosulfate solution (200 mL) was added. The product was extracted with EtOAc (300 mL), the solvent was removed in vacuo and the residue was purified by silica gel chromatography (120 g, 0-50% EtOAc in isohexanes) to afford 2-chloro-5-iodo-1,3-dimethoxybenzene (3) (7.16 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447028B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-a7e27046576a44458eb50d74d470fc8c |
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| Source note | uspto-grants-2016_09 |
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