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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583745Generated: October 26, 2026

Benzene → 6-Phenylhexanenitrile

https://huagongshe.com/reaction/1583745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant6-BromohexanenitrileHCID 81093—
ReactantAluminum(III) ChlorideHCID 6451240—
Product6-PhenylhexanenitrileHCID 1046478286%

Reaction Steps

A solution of 50.0 g (.284 mole) of 6-bromocapronitrile in 550 ml of benzene was cooled to 5° C. and to this was added 77.3 g (.580 mole) of anhydrous aluminum chloride in portions over a 10 minute period. The ice bath was removed and the vigorously stirred mixture was warmed slowly to reflux. After 2 hours at reflux, the mixture was cooled to room temperature, then poured slowly into a mixture of 50 ml of concentrated hydrochloric acid and 250 ml of ice water. The layers were separated and the aqueous portion was extracted twice with 125 ml portions of ether. The combined organic extracts were washed with 100 ml of saturated sodium bicarbonate solution, 100 ml of saturated sodium chloride solution, then dried over sodium sulfate, filtered, and evaporated leaving 53 g of a crude red/brown oil. Distillation under reduced pressure afforded 42.4 g (86%) of the nitrile as a pale yellow oil, bp 136°-140° C./2.5 mm of Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04554276
Source datasetuspto-grants-1985_11
ORD IDord-c0eee28a4db44a8caf985554c8bb086c
Source noteuspto-grants-1985_11