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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033472Generated: October 27, 2026

Benzene → 7-Piperidinoheptanenitrile

https://huagongshe.com/reaction/1033472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantChloroformHCID 6212—
ReactantPiperidineHCID 8082—
ReactantHeptanenitrile, 7-bromo-HCID 88737—
SolventDiethyl EtherHCID 3283—
Product7-PiperidinoheptanenitrileHCID 15030043—

Reaction Steps

In a flask equipped with a dropping funnel and a cooler was placed a mixture of 8.94 g of piperidine, 7.7 ml of benzene and 1.5 ml of chloroform. The mixture was refluxed by heating, and to the mixture was dropwise added 9.50 g of 7-bromoheptanenitrile. After the addition was complete, the mixture was further refluxed by heating for 4 hours and then cooled under ambient condition. To the mixture was added ether, and the resulting mixture was stirred for a while. The reaction mixture was filtered to remove insolubles. The insolubles were washed with ether. The filtrate and washings were combined and concentrated under reduced pressure. The residue was distilled under reduced pressure to give 7-piperidinoheptanenitrile as a colorless oil, yield: 8.92 g (theoretical yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310902
Source datasetuspto-grants-1994_05
ORD IDord-b3e336cd81e04ccd9cc4bb61600eaf69
Source noteuspto-grants-1994_05