HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-(2-Chloroethyl)-4-(2-fluorophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(2-Hydroxyethyl)-4-(2-fluorophenyl)piperazine | HCID 20635175 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(2-Chloroethyl)-4-(2-fluorophenyl)piperazine | HCID 22074917 | 18% |
Reaction Steps
Thionyl chloride (1 mL) was added dropwise to an ice-cooled solution of 1-(2-hydroxyethyl)-4-(2-fluorophenyl)piperazine (300 mg) and pyridine (1 mL) in benzene (20 mL). After 30 minutes the solution was brought to room temperature and then the flask was immersed in a 60° C. oil bath for 1 hour. The layers were separated and the aqueous fraction was extracted with ethyl acetate (2×20 mL). The combined organic fractions were dried over sodium sulfate and the solvent was removed in vacuo, giving the desired product as a yellow solid (58.6 mg, 18%). ESI-MS m/z 243 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706716B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-532bea074d9349e1aa5ec78b82267267 |
| Source note | uspto-grants-2004_03 |