HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 2-Thiophen-2-yl-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Oxo-2-(thiophen-2-yl)acetaldehyde | HCID 5272214 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Thiophen-2-yl-piperazine | HCID 2771726 | 56.7% |
Reaction Steps
A solution of 8.2 g of ethylenediamine in 250 ml of ethanol was added to a solution of 17.64 g of the above aldehyde in 250 ml of ethanol at 0° C. This mixture was stirred at room temperature for 1.5 hours, recooled to 0° C. and 9.6 g of sodium borohydride was added. This mixture was stirred overnight, quenched with water and the ethanol removed. The residue was extracted with dichloromethane, washed with water, dried and evaporated. The residue was crystallized with ether-hexane, giving 12 g of 2-(2-thienyl)piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210193 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-03c5b5351a4a4e46b13c65bdb72b76ca |
| Source note | uspto-grants-1993_05 |