HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Urea → Benzene, 1,3-dichloro-2-iodo-5-nitro-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Urea | HCID 1176 | — |
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | 2,6-Dichloro-4-nitroaniline | HCID 7430 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | Benzene, 1,3-dichloro-2-iodo-5-nitro- | HCID 112948 | 86% |
Reaktionsschritte
To a stirred suspension of 2,6-dichloro-4-nitroaniline (200 g) in glacial acetic acid (1.3 l) at 16° was added dropwise a solution of sodium nitrite (93.84 g) in concentrated sulphuric acid (500 ml), keeping the reaction mixture below 22°. The reaction mixture was stirred and kept below this temperature for 0.5 hour, then poured slowly onto crushed ice/water (2.5 liters) containing urea (31.71 g), keeping the mixture below 23°. Potassium iodide (225.77 g) in water (600 ml) was slowly added with stirring and the mixture stirred at room temperature for 3 hours. The product was filtered off, washed with water then triturated with hot ethanol to give 3,5-dichloro-4-iodonitrobenzene (263.4 g, 86%) as a buff solid, m.p. 147°-150°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04766121 |
| Quelldatensatz | uspto-grants-1988_08 |
| ORD ID | ord-d40584a550694b0d8cc6ab48dd8e4ad1 |
| Quellennotiz | uspto-grants-1988_08 |