HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(thiophen-2-yl)piperazine-1-carboxylate → 1-Methyl-3-(thiophen-2-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(thiophen-2-yl)piperazine-1-carboxylate | HCID 2771741 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methyl-3-(thiophen-2-yl)piperazine | HCID 13048186 | — |
Reaction Steps
A solution of ethyl 3-(2-thienyl)piperazine-carboxylate (27.2 g, 0.11 mol; Preparation 2) in diethyl ether (300 ml) is added to a stirred suspension of lithium aluminum hydride (10.8 g, 0.28 mol) in diethyl ether (1300 ml). The mixture is refluxed for 12 h, cooled to room temperature and worked up as described in "Reagents for Organic Synthesis" , Fieser, L. F. and Fieser, M., John Wiley and Sons, Inc., New York, N.Y. 1967, p. 583. The ether solution is dried (potassium carbonate) and evaporated to give 1-methyl-3-(2-thienyl)piperazine as a light yellow oil, which is characterized as the maleate salt (m.p. 123°-124.5° C.), which is prepared in the manner described in Preparation 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515792 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-0463835542f8453ea4640b1ef8cf8d9f |
| Source note | uspto-grants-1985_05 |