HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[4-(Pyridin-2-yl)piperazin-1-yl]ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Pyridyl)piperazine | HCID 94459 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-(Pyridin-2-yl)piperazin-1-yl]ethan-1-ol | HCID 10512528 | — |
Reaction Steps
To a mixture of 1-(2-pyridyl)piperazine (5 g), potassium carbonate powder (9 g) and N,N-dimethylformamide (30 ml) was added dropwise ethylene bromohydrin (5.74 g) under stirring. The mixture was stirred at room temperature for 6 hours, diluted with water (100 ml) and extracted with chloroform. The chloroform layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was purified by silica gel chromatography [eluent: dichloromethane-methanol (95:5)] to give 4-(2-pyridyl)-1-piperazineethanol as crystals, m.p. 82.5°-84° C. Yield 4.68 g (73.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892875 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-44d5b29f22d548d6aa2835fc66fedf15 |
| Source note | uspto-grants-1990_01 |