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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601455Generated: October 26, 2026

Hydrochloric Acid → 1-Iodo-4-octylbenzene

https://huagongshe.com/reaction/601455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantSodium ThiosulfateHCID 24477—
Reactant4-OctylanilineHCID 85346—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-Iodo-4-octylbenzeneHCID 11594836—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902363B2
Source datasetuspto-grants-2011_03
ORD IDord-1f1013ac3331462c969c553ef7c27cc5
Source noteuspto-grants-2011_03