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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13876생성일: 2026년 10월 24일

Chlorobenzene → Heptylbenzene

https://huagongshe.com/ko/reaction/13876

반응식

참여 물질

역할이름HCID투입량
반응물ChlorobenzeneHCID 7964—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178443917HCID 178443917—
촉매ZincchlorideHCID 3007855—
용매TolueneHCID 1140—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HeptylbenzeneHCID 14115—

반응 단계

A 50-ml four-necked flask was equipped with a stirrer, a thermometer, a dropping funnel and a reflux condenser. 1.090 g (8 mmol) of zinc chloride and 4 ml of N-methylpyrrolidinone were weighed in the flask. The flask was purged with argon, followed by stirring. 3.5 ml (7 mmol) of 2M tetrahydrofuran solution of n-heptylmagnesium chloride was added dropwise at 25° C. over a period of 30 minutes, followed by stirring at 25° C. for 30 minutes. The reaction liquid previously obtained was added, followed by stirring at 25° C. for 30 minutes. Further, 0.558 g (5 mmol) of chlorobenzene was added, followed by stirring at 120° C. for 16 hours. After the completion of the reaction, 10 ml of toluene and 10 ml of saturated aqueous ammonium chloride solution were added, followed by separation. The organic phase was purified by column chromatography to afford 0.684 g of 1-phenylheptane (yield: 78 mol % based on chlorobenzene). The identification of the product was made by mass spectroscopy.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728176B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d6d8dc9dc579454b9f6e82263ada90ec
출처 메모uspto-grants-2010_06