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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223357Generated: October 30, 2026

1-(2-Methoxyphenyl)piperazine → HCID 12961751, compound

https://huagongshe.com/reaction/223357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantHCID 12961745HCID 12961745—
SolventEthanolHCID 702—
ProductHCID 12961751HCID 12961751—

Reaction Steps

7.3 g (0.033 mole) of 2,3-epoxypropoxy-2-(1,3,4-oxadiazol-2-yl)-benzene from Example VII and 6.4 g (0.033 mole) of 2-methoxy-phenylpiperazine in 50 ml of ethanol are refluxed for 17 hours. The solvent is stripped off on a rotary evaporator and the oily residue is taken up in methylene chloride. The solution is washed with 3×50 ml of water, dried over anhydrous sodium sulfate, filtered and concentrated. 12.6 g (93% of theory) of a pale yellow oil are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04353904
Source datasetuspto-grants-1982_10
ORD IDord-470fcc4c4f994e69a2cc0b9ead3bbe57
Source noteuspto-grants-1982_10