HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(4-Bromophenyl)-4-(methylsulfonyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-(4-Bromophenyl)piperazine hydrochloride | HCID 14422838 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Bromophenyl)-4-(methylsulfonyl)piperazine | HCID 21919384 | 81.1% |
Reaction Steps
To a solution of 1-(4-bromophenyl)piperazine hydrochloride (5.09 g, 18.3 mmol) and triethylamine (7.67 ml) in dichloromethane (100 ml) was added methanesulfonyl chloride (2.83 ml, 36.3 mmol) dropwise. The mixture was stirred for 1 hour at room temperature then dichloromethane (100 ml) was added. The organics were washed with water (2×), brine and dried (Na2SO4) and evaporated in vacuo to a yellow solid which crystallised from Ethanol and washed with diethyl ether to give 1-(4-bromophenyl)-4-(methanesulfonyl)piperazine (4.74 g, 81% yield) as a white fluffy powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734183B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-9b5d43c2bcea46638ff80a92281deb53 |
| Source note | uspto-grants-2004_05 |