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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241580Generated: October 30, 2026

Piperazine → 6-Chloro-3-(piperazin-1-yl)benzo[d]isoxazole

https://huagongshe.com/reaction/241580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium HydroxideHCID 14798—
Reactant3,6-Dichlorobenzo[d]isoxazoleHCID 13568449—
Product6-Chloro-3-(piperazin-1-yl)benzo[d]isoxazoleHCID 1356845171.1%

Reaction Steps

3,6-dichlorobenzisoxazole (5.2 g, 27.8 mmol), and anhydrous piperazine (24 g, 278 mmol) are placed in an egg type flask and react at 120° C. for 24 hours. After completion of the reaction, 52 ml of an ice-water mixture is added for quenching the reaction. Further 15 ml of 50% NaOH solution is added to the reaction solution. The reaction solution is stirred for 5 minutes and extracted with dichloromethane (30 ml×3). The dichloromethane layer is combined, washed with 20 ml of saturated saline, dried over anhydrous MgSO4, evaporated to dryness, and subjected to a separation on a column of alumina (200-300 mesh), eluting with dichloromethane:methanol-100:1, to obtain 4.7 g of 6-chloro-3-piperazinyl-benzisoxazole, with a yield of 71%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653069B2
Source datasetuspto-grants-2014_02
ORD IDord-736d716173fd49f089f5651ed616c9c1
Source noteuspto-grants-2014_02