HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596853Generated: October 26, 2026
Triethylamine → 1-Diethylamino ethyl-2-phenyl-3-keto piperazine
https://huagongshe.com/reaction/596853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethylaminoethyl chloride | HCID 13364 | — |
| Reactant | 3-Phenylpiperazin-2-one | HCID 250681 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Diethylamino ethyl-2-phenyl-3-keto piperazine | HCID 21448535 | 64% |
Reaction Steps
144 g. of 2-phenyl-3-keto piperazine are boiled under reflux with 121 g. of diethylamino ethylchloride, 340 cc. of triethylamine, and 1600 cc. of acetone for 24 hours. The cooled solution is filtered to remove triethylamine hydrochloride and the filtrate is evaporated to dryness. The residue is dissolved in water, 40 % sodium hydroxide solution is added thereto, and the oil which forms as upper layer, is extracted with benzene. The benzene solution is dried over anhydrous potassium carbonate, the benzene is removed by distillation, and the residue is distilled in a vacuum. A light yellow, viscous oil of the boiling point 175° C./0.05 mm. Hg is obtained. The oil is twice recrystallized from n-heptane. 145 g. of the above mentioned compound melting at 53°-56° C. are obtained. The yield is 64 % of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04012389 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-41e0dcda606e4611ad34a038ae6032bf |
|---|
| Source note | uspto-grants-1977_03 |
|---|