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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 601455Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1-Iodo-4-octylbenzene

https://huagongshe.com/de/reaction/601455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium IodideHCID 4875—
EduktSodium ThiosulfateHCID 24477—
Edukt4-OctylanilineHCID 85346—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-Iodo-4-octylbenzeneHCID 11594836—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of 4-octylaniline (80.0 g, 389.6 mmol) in water (780 mL) was added aqueous HCl (40 mL) at room temperature. After the mixture was cooled to 0° C., more aqueous HCl (43 mL) was added, followed by dropwise addition of a solution of NaNO2 (26.9 g, 389.6 mmol) in water (195 mL). To the resulting arenediazonium salt solution was added dropwise a solution of potassium iodide (64.67 g, 389.6 mmol) in water (195 mL). The resulting mixture was heated with stirring at 40° C. After two hours, sodium thiosulfate was added to decolorize and the product was extracted with ether. The ethereal extract was washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to give a crude oil. The crude material was dissolved in ether and filtered through a plug of silica gel three times and dried in vacuo to give 1-iodo-4-octylbenzene as a colorless oil. The product was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902363B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-1f1013ac3331462c969c553ef7c27cc5
Quellennotizuspto-grants-2011_03