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HRID 13876作成日:2026年10月25日

Chlorobenzene → Heptylbenzene

https://huagongshe.com/reaction/13876

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorobenzeneHCID 7964—
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178443917HCID 178443917—
触媒ZincchlorideHCID 3007855—
溶媒TolueneHCID 1140—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物HeptylbenzeneHCID 14115—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728176B2
出典データセットuspto-grants-2010_06
ORD IDord-d6d8dc9dc579454b9f6e82263ada90ec
出典メモuspto-grants-2010_06