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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788670Generated: November 3, 2026

Water → 1-(1,3-Benzodioxol-5-YL)-3-(4-phenyl-1-piperazinyl)-1-propanone

https://huagongshe.com/reaction/1788670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-PhenylpiperazineHCID 7096—
ReactantTriethylamineHCID 8471—
Reactant1-(1,3-benzodioxol-5-yl)-3-chloropropan-1-oneHCID 270594—
SolventDimethylformamideHCID 6228—
Product1-(1,3-Benzodioxol-5-YL)-3-(4-phenyl-1-piperazinyl)-1-propanoneHCID 67624584%

Reaction Steps

5-(3-Chloropropionyl)-1,3-benzodioxole (3 g) and N-phenylpiperazine (2.4 g) were dissolved in DMF (20 ml), triethylamine (1.7 g) was then added and the mixture was stirred for 10 hours at room temperature. After completion of the reaction, the reaction mixture was poured into water and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was crystallized from methanol and the resulting crystals were recrystallized from ethanol to give 5-[3-(4-phenyl-1-piperazinyl)propionyl]-1,3-benzodioxole (4.0 g, 84% yield). The characteristics of this compound are shown in Table 3 as Compound 47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684651
Source datasetuspto-grants-1987_08
ORD IDord-117875f1ff4345cb90ccb856fbe3a579
Source noteuspto-grants-1987_08