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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35287Erstellt: 23. Oktober 2026

Urea → Benzene, 1,3-dichloro-2-iodo-5-nitro-

https://huagongshe.com/de/reaction/35287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktUreaHCID 1176—
EduktPotassium IodideHCID 4875—
Edukt2,6-Dichloro-4-nitroanilineHCID 7430—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
ProduktBenzene, 1,3-dichloro-2-iodo-5-nitro-HCID 11294886%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04766121
Quelldatensatzuspto-grants-1988_08
ORD IDord-d40584a550694b0d8cc6ab48dd8e4ad1
Quellennotizuspto-grants-1988_08