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HRID 601455作成日:2026年10月24日

Hydrochloric Acid → 1-Iodo-4-octylbenzene

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium IodideHCID 4875—
反応物Sodium ThiosulfateHCID 24477—
反応物4-OctylanilineHCID 85346—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物1-Iodo-4-octylbenzeneHCID 11594836—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902363B2
出典データセットuspto-grants-2011_03
ORD IDord-1f1013ac3331462c969c553ef7c27cc5
出典メモuspto-grants-2011_03