HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592992Generated: October 30, 2026
Potassium Iodide → 3-Iodo-5-(methoxycarbonyl)benzoic acid
https://huagongshe.com/reaction/1592992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-Amino-5-(methoxycarbonyl)benzoic acid | HCID 13557643 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Iodo-5-(methoxycarbonyl)benzoic acid | HCID 15840391 | 55.1% |
Reaction Steps
To an ice-cold, stirred solution of commercially available 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in 2 N hydrochloric acid (156 mL) was added a solution of sodium nitrite (1.84 g, 26.67 mmol) in water (10.8 mL). This mixture was then added dropwise to an ice-cold, stirred solution of potassium iodide (8.84 g, 53.25 mmol) in water (26.2 mL). After stirring for 35 min, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium thiosulfate, and saturated sodium chloride, dried (sodium sulfate), and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50:50:2 hexanes/ethyl acetate/acetic acid) afforded the title compound (4.48 g, 55% yield) as an off-white solid. ESI-MS (m/z): 305 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294642B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-f95ee87fc6c347dd90c872a903474685 |
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| Source note | uspto-grants-2007_11 |
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