HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530912Erstellt: 25. Oktober 2026
Acetic Acid → 4-Iodo-N1-methylbenzene-1,2-diamine
https://huagongshe.com/reaction/530912
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 4-iodo-N-methyl-2-nitroaniline | HCID 65809849 | — |
| Katalysator | Iron | HCID 23925 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-Iodo-N1-methylbenzene-1,2-diamine | HCID 66064280 | 89,7% |
Reaktionsschritte
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 mixture 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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09353110B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-2c09d1244ae74f059fc05b66611d61f6 |
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| Quellennotiz | uspto-grants-2016_05 |
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