HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(2-Chloro-3-methylphenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloro-m-toluidine | HCID 11412438 | — |
| Reactant | Ethanamine, 2-bromo-N-(2-bromoethyl)-, hydrobromide (1:1) | HCID 12692731 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Chloro-3-methylphenyl)piperazine | HCID 15124093 | 56.1% |
Reaction Steps
To a mixture of 6.08 g of 2-chloro-3-methylaniline, 9 g of di(2-bromoethyl)amine hydrobromide and 4 ml of water was added a solution of 0.8 g of potassium hydorxide and 2.5 ml of water 3 times of 1 hour interval at 100° C., then the reaction mixture was stirred at the same temperature for 9 hours. To the resultant reaction mixture was added potassium hydroxide to make the mixture alkaline, and the mixture was extracted with diethyl ether, washed with water, dried with anhydrous magnesium sulfate. The solvent was removed by evaporation and the residue thus obtained was purified by means of a silica gel column chromatography (eluent: 5%-methanol/chloroform), and obtained 3.41 g of 4-(2-chloro-3-methylphenyl)piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006528 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-bddfb4fad3654e35b394208baaf54b01 |
| Source note | uspto-grants-1991_04 |