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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112738Generated: November 4, 2026

1-Phenylpiperazine → HCID 22762587, compound

https://huagongshe.com/reaction/1112738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 22762545HCID 22762545—
SolventDimethylformamideHCID 6228—
ProductHCID 22762587HCID 22762587—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of N-phenacyl-3-bromopropanamide (10.2 g; 0.038 mole) and N-phenylpiperazine (12.0 g; 0.074 mole) in dry DMF (100 ml) was stirred with anhydrous, finely-powdered sodium carbonate (15.0 g) for 18 hours at room temperature. The temperature was then increased to 80° C. and held for 12 hours to complete the reaction. The DMF was evaporated off under vacuum and the residue diluted with water (100 ml). The mixture was extracted with chloroform (3 × 100 ml). The extracts were shaken with 2 × 100 ml 2N HCl and the organic layer discarded. The aqueous layer was basified with NaOH solution to pH 9 and extracted with 3 × 75 ml CHCl3. The extracts were washed with water and dried. After removal of the solvent the remaining viscous gum triturated with ether to give a buff-coloured solid. After recrystallisation from isopropanol the product weighed 6.0 g and melted at 126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123529
Source datasetuspto-grants-1978_10
ORD IDord-ab5c6fe7e50e4cf4bedafb686dac64ff
Source noteuspto-grants-1978_10