HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 20382048, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-chloro-3-phenoxypyridine | HCID 11217985 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20382048 | HCID 20382048 | — |
Reaction Steps
To a solution of 10.5 g of 2-chloro-3-phenoxypyridine in 25 ml of n-butanol is added 20 g of piperazine and the solution is refluxed for 24 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-2-piperazinylpyridine; bp, 115°-117° C./0.15 mm, crystallized and has a mp 56°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179563 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-2503f11c042b4da785ca0f6cae2f41b1 |
| Source note | uspto-grants-1979_12 |