HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499667Generated: October 31, 2026
Water → 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone
https://huagongshe.com/reaction/1499667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 5'-Chloro-2'-hydroxy-4'-methylacetophenone | HCID 598229 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(5-Chloro-2-hydroxy-3-iodo-4-methylphenyl)ethanone | HCID 11472394 | 97% |
Reaction Steps
To a stirred solution of 1-(5-chloro-2-hydroxy-4-methylphenyl)ethanone (from Oakwood, 50.0 g, 271 mmol) in acetic acid (300 mL) was added N-iodosuccinimide (73.1 g, 325 mmol) and the resulting mixture was stirred on a heating mantle between 60˜80° C. over 3.5 hours then cooled to room temperature and stirred overnight. Water (500 mL) was added to the mixture in portions, which caused a dark solid to form. After stirring for 10 minutes, the solids were filtered, washing with additional water. The light to dark brown solids were dried under vacuum for 4 hours then air dried over the weekend to give 81.3 g (97%) of the desired product. LCMS calculated for C9H9ClI2 (M+H)+: m/z=310.9; Found: 311.0. 1H NMR (300 MHz, CDCl3): δ 13.21 (s, 1H), 7.71 (s, 1H), 2.65 (s, 3H), 2.63 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-aeb346245a894854b83f85c2ff78525c |
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| Source note | uspto-grants-2015_12 |
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