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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500543Generated: October 31, 2026

Piperazine → 1-(1-Benzothiophen-4-yl)piperazine hydrochloride

https://huagongshe.com/reaction/1500543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant4-Chloro-1-benzothiopheneHCID 12398605—
ReactantTri-tert-butylphosphonium TetraphenylborateHCID 23136663—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
Product1-(1-Benzothiophen-4-yl)piperazine hydrochlorideHCID 57482541—

Reaction Steps

4-Chlorobenzo[b]thiophene (5.00 g), piperazine (5.11 g), palladium acetate (II) (2.7 mg), tri-tert-butylphosphonium tetraphenylborate (6.2 mg), sodium tert-butoxide (8.548 g), and xylene (70 ml) were stirred at 120 to 130° C. for 5 hours. After the reaction mixture was cooled to room temperature, water was added thereto, and the layers were separated. The xylene layer was washed with water, and then with saline. After addition of activated carbon, the mixture was stirred at room temperature for 30 minutes. After filtration of the mixture, concentrated hydrochloric acid was added to the filtrate, and the resulting mixture was stirred at room temperature for 30 minutes. The precipitated crystals were collected by filtration and dried to obtain 4-(1-piperazinyl)benzo[b]thiophene hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206169B2
Source datasetuspto-grants-2015_12
ORD IDord-3d1138d97cb1485ca7def65d04daf19c
Source noteuspto-grants-2015_12