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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4-Chloro-1-benzothiophene | HCID 12398605 | — |
| Reactant | Tri-tert-butylphosphonium Tetraphenylborate | HCID 23136663 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206169B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-3d1138d97cb1485ca7def65d04daf19c |
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| Source note | uspto-grants-2015_12 |
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