HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273322Generated: October 25, 2026
Acetic Acid → 4-Iodo-N1-methylbenzene-1,2-diamine
https://huagongshe.com/reaction/2273322
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-iodo-N-methyl-2-nitroaniline | HCID 65809849 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Iodo-N1-methylbenzene-1,2-diamine | HCID 66064280 | 89.7% |
Reaction Steps
A mixture of an iron powder (1.7 g), acetic acid (2.2 ml), ethanol (80 ml), and water (25 ml) was stirred at 70° C. To the reaction mixture was added dropwise a mixture of (4-iodo-2-nitro-phenyl)-methyl-amine (2.0 g) and ethanol (20 ml). After that, the mixturee was stirred at 70° C. for 6 hours. Then, the reaction mixture was filtrated and thoroughly washed with THF. The resulting filtrate was concentrated under reduced pressure. To the resulting residue was poured saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 4-iodo-N1-methyl-benzene-1,2-diamine (1.6 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120823B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8e31494b2f79435f87da827da6172e50 |
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| Source note | uspto-grants-2015_09 |
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