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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733266Generated: November 1, 2026

Piperidine → 1-[3-(p-Tert.butyl-phenyl)-2-methyl-2-propenyl]-piperidine

https://huagongshe.com/reaction/1733266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-(p-Tert.butyl-phenyl)-2-methyl-allyl bromideHCID 57204175—
SolventDiethyl EtherHCID 3283—
Product1-[3-(p-Tert.butyl-phenyl)-2-methyl-2-propenyl]-piperidineHCID 57105769—

Reaction Steps

35 g of 3-(p-tert.butyl-phenyl)-2-methyl-allyl bromide in 70 ml of ether are added dropwise to a solution of 24.5 g of piperidine in 100 ml of absolute ether and the mixture is heated at reflux for 16 hours. The piperidine hydrobromide is removed by filtration and rinsed with ether. The ether solution is extracted with 2-N hydrochloric acid and made alkaline with 50% sodium hydroxide. The alkaline-aqueous solution is again extracted with ether, washed with water, dried over sodium sulphate and evaporated. By distillation there is obtained pure 1-[3-(p-tert.butyl-phenyl)-2-methyl-2-propenyl]-piperidine of boiling point 96°-98° C./0.03 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241058
Source datasetuspto-grants-1980_12
ORD IDord-d4413a4440cb404099fed1e0568d214c
Source noteuspto-grants-1980_12