HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 70504599, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenesulfinyl chloride | HCID 4190003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70504599 | HCID 70504599 | — |
Reaction Steps
To a solution of 4.87 g of N-phenylpiperazine in 150 ml of dichloromethane containing 4.59 ml of triethylamine is added dropwise with stirring under nitrogen a solution of 4.82 g of benzenesulfinyl chloride in 50 ml of dichloromethane. The reaction mixture is stirred for 3 hours at room temperature, diluted with 100 ml of dichloromethane and washed with 150 ml of water and 100 ml of 5% potassium carbonate solution. The organic layer is dried over anhydrous sodium sulfate and evaporated in vacuo to a nearly colorless crystalline solid. Recrystallization from ethanol affords 6.37 g of 1-phenylpiperazine-4-benzenesulfinamide as a nearly colorless crystalline solid, mp, 101°-104° (softens 98°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04425342 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-24acb2bef74e4a7da78631e1b19d002d |
| Source note | uspto-grants-1984_01 |