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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371995Generated: October 27, 2026

Chlorosuccinimide → 1-(2-Chloro-5-methoxyphenyl)piperazine hydrochloride

https://huagongshe.com/reaction/1371995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant1-(3-Methoxyphenyl)piperazine dihydrochlorideHCID 81429—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-(2-Chloro-5-methoxyphenyl)piperazine hydrochlorideHCID 21070973—

Reaction Steps

To a solution of 5.3 g (20 mmol) of 1-(3-Methoxyphenyl)piperazine dihydrochloride in 120 mL of acetic acid and 30 mL of water at 0° C. was added 3.3 g (20 mmol) of N-chlorosuccinimide. After 5 hours, the reaction was concentrated to an oil in vacuo, and the oil was partitioned between ethyl acetate and 1M NaOH. The phases were separated, and the ethyl acetate phase was washed once each with water and brine, dried over Na2SO4, filtered, and the filtrate was concentrated to an oil in vacuo. The oil was dissolved in a minimum volume of methanol, and the solution was acidified with 2M HCl in ether. The product was isolated by filtration. 1H NMR (D2O, 400 MHz) 7.28 (d, 1H), 6.66 (m, 3H), 3.70 (s, 3H), 3.32 (m, 4H), 3.20 (m, 4H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157464B2
Source datasetuspto-grants-2007_01
ORD IDord-acaee8e10bc74fdeb324de8cb6118e97
Source noteuspto-grants-2007_01