HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54308Erstellt: 24. Oktober 2026
4,5-Difluoro-2-nitroaniline → 1,2-Diamino-4,5-difluorobenzene
https://huagongshe.com/de/reaction/54308
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4,5-Difluoro-2-nitroaniline | HCID 157151 | — |
| Edukt | 4-Fluorobenzene-1,2-diamine | HCID 164584 | — |
| Edukt | Calcium Chloride | HCID 5284359 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,2-Diamino-4,5-difluorobenzene | HCID 2736755 | — |
Reaktionsschritte
4,5-Difluoro-1,2-diaminobenzene was prepared using an adaptation of the method of Tsuji et al., (Tsuji, Y. et al., J. Org. Chem. 55:580 (1990)). Zn powder (942 mg, 14.4 mmol), CaCl2 (94.4 mg), H2O (1.0 mL) and 4.0 mL EtOH were combined and brought to reflux as described for 4-fluoro-1,2-diaminobenzene (see Example 11) and to this mixture was added slowly dropwise a solution of 4,5-difluoro-2-nitroaniline (200 mg, 1.15 mmol) in 2 mL EtOH. Analysis and workup were as described for 4-fluoro-1,2-diaminobenzene (Example 11) except that the reaction was dissolved in 5 mL H2O and the solution extracted with 3×10 mL Et2O. The organic layers were combined and treated with activated charcoal, dried (MgSO4) and filtered through a pad of Celite. The solvent was evaporated at reduced pressure to yield 111.5 mg (67.3%) of a brown crystalline solid. 1H NMR (CDCl3) δ3.34 (br s, 4H, NH2), 6.53 (t, 2H, ArH).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05622952 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-cedfbb40da604e36b7e49d168acf96bb |
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| Quellennotiz | uspto-grants-1997_04 |
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