HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-[3-(p-Tert.butyl-phenyl)-2-methyl-2-propenyl]-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-(p-Tert.butyl-phenyl)-2-methyl-allyl bromide | HCID 57204175 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[3-(p-Tert.butyl-phenyl)-2-methyl-2-propenyl]-piperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04241058 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-d4413a4440cb404099fed1e0568d214c |
| Source note | uspto-grants-1980_12 |