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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343588Generated: October 31, 2026

Piperazine → 3-(1-Piperazinyl)-1,2-benzisothiazole

https://huagongshe.com/reaction/343588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantChlorobenzeneHCID 7964—
Reactant3-Chloro-1,2-benzisothiazoleHCID 598190—
SolventEthylene GlycolHCID 174—
Product3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 277214492.3%

Reaction Steps

215.4 g (2.50 mol) of piperazine, 50.0 g of chlorobenzene, 100.0 g of ethylene glycol were placed in a four-neck 1000 ml flask equipped with a stirrer, a thermometer, a dropping funnel and a condenser, 169.5 g (1.00 mol) of 3-chloro-1,2-benzisothiazole was added dropwise in the melted state at about 120° C. over 1 hour while stirring, which was thereafter stirred for 2 hours to complete the reaction. After excess piperazine was removed with water, the reaction mixture was made acidic with hydrochloric acid, extracted into an aqueous layer, which was made alkaline with aqueous sodium hydroxide to obtain 202.4 g (m.p. 89°-90° C.) of 3-(1-piperazinyl)-1,2-benzisothiazole as crystals. Yield from 3-chloro-1,2-benzisothiazole was 92.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861511
Source datasetuspto-grants-1999_01
ORD IDord-ede2007e863e491c91da20a282468f06
Source noteuspto-grants-1999_01