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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601455생성일: 2026년 10월 23일

Hydrochloric Acid → 1-Iodo-4-octylbenzene

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium IodideHCID 4875—
반응물Sodium ThiosulfateHCID 24477—
반응물4-OctylanilineHCID 85346—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1-Iodo-4-octylbenzeneHCID 11594836—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902363B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-1f1013ac3331462c969c553ef7c27cc5
출처 메모uspto-grants-2011_03