HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61873Generated: October 28, 2026
Sulfuric Acid → 4-Ethyl-3-iodo-alpha,alpha-dimethylbenzeneacetic acid
https://huagongshe.com/reaction/61873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-(4-Ethylphenyl)-2-methylpropanoic acid | HCID 58128446 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Ethyl-3-iodo-alpha,alpha-dimethylbenzeneacetic acid | HCID 66834609 | — |
Reaction Steps
2-(4-Ethylphenyl)-2-methylpropanoic acid (58.1 g, 302.2 mmol) was dissolved in acetic acid (175 ml), added with N-iodosuccinimide (71.4 g, 317.3 mmol, 1.05 eq.) and conc. sulfuric acid (75 ml) at 0° C. Thereafter, the mixture was stirred at room temperature for 2 hrs. After cooling the reaction solution to 0° C., 10% aqueous solution of sodium hydrogen sulfite (100 ml) was added and the mixture was stirred for 1 hr. H2O (450 ml) was added to the mixture and the precipitated solid was filtered to obtain the title compound as a crude product. Ethanol (150 ml) and 10% aqueous solution of sodium hydrogen sulfite (50 ml) were added to the crude product, and the mixture was dissolved under heating at 50° C. After confirming the dissolution, the solution was cooled to room temperature, added with H2O (300 ml), and then stirred at 0° C. for 1 hr. The precipitated solid was filtered to obtain the title compound (95.8 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440922B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-7ecfbe74d2a1453daec63b9ce67009ba |
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| Source note | uspto-grants-2016_09 |
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