HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 1-Benzyl-4-tert-butyl-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine, 2',2''-dichloro-1,1-dimethyl- | HCID 96167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Benzyl-4-tert-butyl-piperazine | HCID 3591937 | — |
Reaction Steps
A solution of 2000 g of bis-(2-chloroethyl)-tert-butylamine in 500 cc of ethanol and a solution of 1095 g of benzylamine in 750 cc of ethanol are simultaneously added dropwise to 1000 cc of boiling ethanol. After the addition is complete, the reaction mixture is heated to the boil for 1 hour. The mixture is subsequently concentrated in a vacuum and the residue is dissolved in dilute hydrochloric acid. The acid solution is washed with ether and is subsequently rendered alkaline with a concentrated, aqueous sodium hydroxide solution. The liberated base is extracted with ether and the ether residue is distilled. 1-benzyl-4-tert-butyl piperazine has a B.P. of 160°-162° at 12 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962248 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-b0a805842af4428eaa3f82b69830ea24 |
| Source note | uspto-grants-1976_06 |