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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638560Generated: October 30, 2026

1-Phenylpiperazine → HCID 13537610, compound

https://huagongshe.com/reaction/638560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 20252669HCID 20252669—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventAcetone diethyletherHCID 21584533—
ProductHCID 13537610HCID 13537610102.9%

Reaction Steps

A solution of 3.5 g of (5-bromomethylisoxazol-3-yl)-phenylmethanone in 100 ml of Et2O was added dropwise to a solution of 8.6 g of phenylpiperazine in 375 ml of 20% acetone/Et2O. The resulting mixture was stirred at room temperature for 72 hours. This mixture was washed with water and brine, and dried over MgSO4. Concentration of the product gave an oil, which was taken up in 500 ml of CH2Cl2 and stirred with 20 g of silica gel overnight. The silica was removed by filtration and washed with 500 ml of CH2Cl2. The combined filtrates were concentrated to give 4.7 g of an oil which solidified on standing. Recrystallization from ethanol yielded 3.1 g (69%) of platelets, m.p. 100°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562187
Source datasetuspto-grants-1985_12
ORD IDord-9a33bd7f6971474695ec3cc355b17aea
Source noteuspto-grants-1985_12