HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239858Generated: November 3, 2026
Hydrochloric Acid → 2-Chloro-1-iodo-4-(methylsulfonyl)benzene
https://huagongshe.com/reaction/239858
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzenamine, 2-chloro-4-(methylsulfonyl)- | HCID 25801 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-1-iodo-4-(methylsulfonyl)benzene | HCID 59350819 | — |
Reaction Steps
2-Chloro-4-Methylsulfonylaniline in a 1:1:3 mixture (0.4 M) of Acetic Acid, Hydrochloric Acid, 37% and Water was cooled to 0° C. and slowly treated with a 4 M solution of sodium nitrite in water. The reaction was stirred at 5° C. for 30 minutes then treated dropwise with a 2M solution of potassium iodide in water. The reaction evolved a gas and turned brown. The reaction was stirred 15 minutes at 0° C., 40 minutes at rt and 1 h at 60° C. The brown solid was filtered, dissolved in ethyl acetate and the solution washed with acidified sodium thiosulfate and then brine. The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. During evaporation, a precipitate appeared and was filtered. The mother liquors were evaporated further and 2 more crops were collected. The last mother liquor was transferred with diethyl ether and upon evaporation yields more products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642799B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-ccb7f8216303491c84585e7787bdf140 |
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| Source note | uspto-grants-2014_02 |
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