HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541294Generated: November 3, 2026
Iodine → 4-Chloro-5-iodo-2-methylbenzoic acid
https://huagongshe.com/reaction/541294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Chloro-2-methylbenzoic acid | HCID 348269 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Chloro-5-iodo-2-methylbenzoic acid | HCID 68288948 | — |
Reaction Steps
To a round-bottom flask was added a solution of 4-chloro-2-methylbenzoic acid (30.0 g, 176 mmol, 1.00 equiv) in acetic acid (300 mL). NaIO4 (19.0 g, 88.8 mmol, 0.50 equiv), I2 (49.0 g, 193 mmol, 1.10 equiv), and sulfuric acid (3 mL) were added to the reaction. The resulting mixture was stirred overnight at 110° C. After cooling to ambient temperature, the reaction was carefully quenched with 500 mL of Na2S2O3 (aq., sat.). The resulting solids were collected by filtration and then dissolved in 500 mL of ethyl acetate. The organic phase was washed with 2×200 mL of brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. This resulted in 20.0 g (38%) of 4-chloro-5-iodo-2-methylbenzoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871790B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-6accd657c61143f78d8345e0113e9818 |
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| Source note | uspto-grants-2014_10 |
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