HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 70607392, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 14044047 | HCID 14044047 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70607392 | HCID 70607392 | — |
Reaction Steps
To a solution of 13 g of 4-chloro-3-phenoxypyridine in 25 ml of methanol is added 30 g of piperazine and the solution is stirred and heated for 72 hours. The resulting mixture is concentrated at reduced pressure. The residue is shaken with 500 ml of ether and excess dilute aqueous sodium hydroxide. The organic phase is separated, dried and filtered. The filtrate is concentrated and the product distilled to give 3-phenoxy-4-piperazinylpyridine; bp 134°-135° C./0.2 mm, solidified and has a mp of 74°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179563 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-9353d9b20bc24c28b049aaa37bd32c0a |
| Source note | uspto-grants-1979_12 |