HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-Piperazineethanol, 4-(3-chlorophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Chlorophenyl)piperazine monohydrochloride | HCID 25681 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Piperazineethanol, 4-(3-chlorophenyl)- | HCID 96703 | 78.6% |
Reaction Steps
Ethylene bromohydrin (5.4 g) was added dropwise to a mixture of 1-(3-chlorophenyl)piperazine hydrochloride (5 g), potassium carbonate powder (12 g) and N,N-dimethylformamide (35 ml) with stirring. The mixture was further stirred at room temperature overnight, then diluted with 100 ml of water and extracted with ethyl ether. The ethyl ether layer was washed with saturated aqueous sodium chloride and dried over Na2SO4. The solvent was distilled off and the residue was purified by silica gel chromatography [eluent: ethyl acetate-methanol (4:1)] to give 4.06 g (78.6%) of 4-(3-chlorophenyl)-1-piperazineethanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603135 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-d59b809d03444a6cb96c5419613064fc |
| Source note | uspto-grants-1986_07 |