HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092279Generated: October 30, 2026
Acetic Acid → 2-Amino-3-iodo-4-methylbenzoic acid
https://huagongshe.com/reaction/2092279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Iodo-4-methyl-2-nitrobenzoic acid | HCID 52987956 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-3-iodo-4-methylbenzoic acid | HCID 45789611 | 96.2% |
Reaction Steps
3-Iodo-4-methyl-2-nitrobenzoic acid (46.00 g, 150 mmol) was suspended in ethanol (500 mL) and acetic acid (86 mL, 1498 mmol). The mixture was heated to 70° C. and iron (33 g, 599 mmol) was added in small portions. Stirring was continued for 3 h, and then the reaction was cooled down to RT and poured on 1.5 kg of crushed ice and 1 L of 5 N aqueous HCl. The mixture was extracted with ethyl acetate and the organic layer was dried with sodium sulfate, concentrated under vacuum and dried to give 2-amino-3-iodo-4-methylbenzoic acid (40 g, 96%) as a tan solid. MS (M+H)+ 278
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440674B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-47a25e384d504983ad19521446e3d516 |
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| Source note | uspto-grants-2013_05 |
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