HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(1-Oxo-2-propenyl)-4-(phenylmethyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(1-Oxo-2-propenyl)-4-(phenylmethyl)piperazine | HCID 15056293 | 13% |
Reaction Steps
A solution of acryloyl chloride (4.52 g, 0.05 mole) in 25 ml of ethyl ether was added to a cold solution of 1-benzylpiperazine (8.8 g, 0.05 mole) and triethylamine (30 ml, 0.20 mole) in 500 ml of ethyl ether. A white precipitate formed. The reaction mixture was stirred overnight, filtered and the precipitate washed well with ethyl ether. The solvent and triethylamine were removed and the product chromatrographed on silica, eluting with ethyl acetate/hexane [30:70(v/v)] to yield 1.5 g of the title compound. The structure was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959364 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-a491197c42204be1af351d49df346060 |
| Source note | uspto-grants-1990_09 |