HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655639Generated: November 1, 2026
Water → 4-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetate
https://huagongshe.com/reaction/655639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| Reactant | 1-(1-Benzothiophen-4-yl)piperazine hydrochloride | HCID 57482541 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetate | HCID 57482549 | 55.5% |
Reaction Steps
1.0 g (3.9 mmol) of 1-benzo[b]thiophen-4-yl-piperazine hydrochloride was suspended in 20 ml of dimethylformamide (DMF), and potassium carbonate (1.3 g, 9.4 mmol) and 4-bromobutyl acetate (0.7 ml, 4.8 mmol) were added thereto. The reaction mixture was stirred at 80° C. for 6 hours, cooled to room temperature, and water was added thereto, and extracted with ethyl acetate. The organic phase was washed with water, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (dichloromethane:methanol=30:1), and concentrated to dryness under reduced pressure to obtain 4-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)butyl acetate (0.72 g) as light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071600B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-d0b9ca50fbfc4892821483abf8a60284 |
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| Source note | uspto-grants-2011_12 |
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