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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13876Generated: October 25, 2026

Chlorobenzene → Heptylbenzene

https://huagongshe.com/reaction/13876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178443917HCID 178443917—
CatalystZincchlorideHCID 3007855—
SolventTolueneHCID 1140—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHeptylbenzeneHCID 14115—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728176B2
Source datasetuspto-grants-2010_06
ORD IDord-d6d8dc9dc579454b9f6e82263ada90ec
Source noteuspto-grants-2010_06