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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638561Generated: October 31, 2026

1-Phenylpiperazine → HCID 13537621, compound

https://huagongshe.com/reaction/638561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 20252673HCID 20252673—
SolventDiethyl EtherHCID 3283—
SolventAcetone diethyletherHCID 21584533—
ProductHCID 13537621HCID 13537621115.6%

Reaction Steps

A solution of 3.7 g of (5-bromomethylisoxazol-3-yl)-4-fluorophenylmethanone in 100 ml of Et2O was added dropwise to a solution of 5.2 g of N-phenylpiperazine in 400 ml of 20% acetone/Et2O. The resulting mixture was stirred at room temperature for 24 hours. This mixture was filtered and the solution was washed with water (2×200 ml) and saturated NaCl, and dried over MgSO4. Concentration of the product gave 5.5 g of a solid which was dissolved in 100 ml of CH2Cl2 and stirred with 5 g of SiO2. This mixture was filtered, the silica washed with CH2Cl2, and the organics were evaporated to give 3.7 g of a solid. The amine was recrystallized from 135 ml of 8% toluene/hexane to yield 2.5 g (53%) of needles, m.p. 94°-95°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562187
Source datasetuspto-grants-1985_12
ORD IDord-4f29ed0a5a6c4a028d9a13ff81ea2ff3
Source noteuspto-grants-1985_12