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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448131Generated: November 2, 2026

Piperazine → HCID 70607392, compound

https://huagongshe.com/reaction/1448131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 14044047HCID 14044047—
SolventMethanolHCID 887—
ProductHCID 70607392HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179563
Source datasetuspto-grants-1979_12
ORD IDord-9353d9b20bc24c28b049aaa37bd32c0a
Source noteuspto-grants-1979_12