HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973101Generated: November 2, 2026
Hydrochloric Acid → 2-Iodo-4-methoxybenzoic acid
https://huagongshe.com/reaction/1973101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Amino-4-methoxybenzoic acid | HCID 351010 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Iodo-4-methoxybenzoic acid | HCID 12822182 | — |
Reaction Steps
150 G. of 4-methoxy-anthranilic acid are suspended at 0° C. in 2 liters of water and 80 ml. of concentrated hydrochloric acid. To this solution is added dropwise with stirring at 0°-5° C. over a period of 30 minutes a solution of 62 g. of sodium nitrite in 130 ml. of water. The resulting diazonium salt solution is stirred for an additional 15 minutes at 0°-5° C. A solution of 164 g. of potassium iodide in 700 ml. of 5-N sulfuric acid is subsequently added dropwise at 3°-6° C. over a period of 45 minutes. Then, the mixture is stirred at room temperature for 30 minutes and heated slowly to reflux. After boiling at reflux for 2 hours, the mixture is cooled to room temperature. The precipitated brown crystals are removed by filtration and washed neutral with water. The filter cake is dried under reduced pressure, and there is obtained 2-iodo-4-methoxy-benzoic acid as brown crystals having a melting point of 174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03996229 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-b8f708161993458cbae37648e8df3436 |
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| Source note | uspto-grants-1976_12 |
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