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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13894Erstellt: 23. Oktober 2026

Chlorobenzene → Heptylbenzene

https://huagongshe.com/de/reaction/13894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorobenzeneHCID 7964—
EduktTetrahydrofuranHCID 8028—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178443917HCID 178443917—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelTolueneHCID 1140—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktHeptylbenzeneHCID 14115—

Reaktionsschritte

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 0.688 g of 1-phenylheptane (yield: 78 mol % based on chlorobenzene). The identification of the product was made by mass spectroscopy.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728176B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-19b373f44095458b882fa7b309cd94ff
Quellennotizuspto-grants-2010_06