HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215133Generated: October 31, 2026
Iodine → 5-Chloro-4-iodo-2-methoxybenzoic acid
https://huagongshe.com/reaction/2215133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Chloro-4-iodo-2-methoxybenzoic acid | HCID 16791858 | 59.6% |
Reaction Steps
A stirred solution of 4-amino-5-chloro-2-methoxy benzoic acid (12.25 g , 60.8 mmol) in water (136 mL ) and concentrated sulfuric acid (34 mL) was cooled to 0° C. in a flask fitted with an overhead stirrer. A solution of sodium nitrite (4.62 g , 66.9 mmol) in water (26 mL) was added dropwise while keeping the internal temperature around 0° C. Potassium iodide (11.11 g , 66.9 mmol) and iodine (4.246 g , 33.5 mmol) were dissolved in water (130 mL) and added dropwise to the stirred reaction mixture. After 2 hours the reaction was extracted with ethyl acetate. The organic extracts were then washed with 10% sodium thiosulfate and brine, then dried over magnesium sulfate, filtered and evaporated to dryness to yield 11.32 g of the title compound, m.p. 150–151° C. This material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109193B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-5f4f748665e04732b21f3bae4913b9e9 |
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| Source note | uspto-grants-2006_09 |
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