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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414006Generated: November 1, 2026

Water → 1-(3-Chlorophenyl)-4-(3-chloropropyl)-piperazine

https://huagongshe.com/reaction/1414006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Chlorophenyl)piperazine monohydrochlorideHCID 25681—
SolventAcetoneHCID 180—
Product1-(3-Chlorophenyl)-4-(3-chloropropyl)-piperazineHCID 1014449%

Reaction Steps

To a solution fo 7.36 g. (0.184 mole) of sodium hydroxide in 75 ml. of water and 75 ml. of acetone there is added 17.16 g. (0.074 mole) of 1-(3-chlorophenyl)piperazine hydrochloride and 11.59 g. (0.074 mole) of 1-bromo-3-chloropropane, and the resulting mixture is stirred at 27° for 18 hrs. The organic layer is then separated and concentrated to an oil under reduced pressure. The oil is treated with hot (85°) 6 N HCl until solution is complete, and the resulting solution is filtered and stored at 5° for 18 hrs. The precipitate which forms is collected on a filter to afford 17.52 g. (87%) of the hydrochloride salt of the product, m.p. 198°-200°. Concentration of the mother liquor under reduced pressure and recrystallization of the residue from water affords an additional 1.82 g (9%) of product, m.p. 196°-198°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04252806
Source datasetuspto-grants-1981_02
ORD IDord-c7af2029361c420c8a72a17142596603
Source noteuspto-grants-1981_02