Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448132Generated: November 4, 2026

Piperazine → HCID 20382048, compound

https://huagongshe.com/reaction/1448132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-chloro-3-phenoxypyridineHCID 11217985—
Solvent1-ButanolHCID 263—
ProductHCID 20382048HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179563
Source datasetuspto-grants-1979_12
ORD IDord-2503f11c042b4da785ca0f6cae2f41b1
Source noteuspto-grants-1979_12