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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583540Generated: October 31, 2026

1-Bromo-3-chloropropane → 1-(3-Fluorophenyl)piperazine

https://huagongshe.com/reaction/1583540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-Fluorophenyl)piperazineHCID 77418—
SolventDimethylformamideHCID 6228—
Product1-(3-Fluorophenyl)piperazineHCID 77418—
ProductHCID 13312914HCID 13312914—

Reaction Steps

The 1-(3-chloropropyl)-4-(3-fluorophenyl piperazine used is prepared in the following manner: 32 g (203 m. moles) of 1-bromo-3-chloropropane are added drop by drop to a mixture of 12.2 g (67.7 m. moles) Of 1-(3-fluorophenyl piperazine [prepared according to D. R. Maxwell and W. R. Wragg, English Pat. No. 943,739, C.A. 60, 5522c (1964)], 9.4 g (68 m. moles) of potassium carbonate and 135 cc of N,N-dimethylformamide. The stirring is continued for 9 hours at ambient temperature. The inorganic products are then removed by filtration, then the filtrate is concentrated under reduced pressure. The residue is dissolved in ether, the solution washed with a saturated solution of sodium chloride, then dried on sodium sulfate. The evaporation of the ether supplies an oil which is distilled (boiling1 =137°-140°). The 1-(3-chloropropyl)-4-(3-fluorophenyl)piperazine is obtained in the form of an oil that is crystallized in hexane. Yield: 11.6 g (67%), Melting point=48°-49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552878
Source datasetuspto-grants-1985_11
ORD IDord-1af4e7bb1b3e4c1ea1208ccd2d76947c
Source noteuspto-grants-1985_11