HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655638Generated: October 31, 2026
Tetrahydrofuran → 3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanol
https://huagongshe.com/reaction/655638
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate | HCID 57482547 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanol | HCID 57482548 | 5% |
Reaction Steps
Lithium aluminum hydride (1.18 g, 24.8 mmol) was added to a solution of 5.26 g (16.5 mmol) of ethyl 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propionate in a tetrahydrofuran (THF) solution (55 ml) under ice cooling, and the mixture was stirred at room temperature for 4 hours. To the reaction solution, water (1.2 ml), 15% aqueous sodium hydroxide solution (1.2 ml), and water (3.6 ml) were added in this order and the mixture was stirred at room temperature. Insoluble matter was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→ethyl acetate) and concentrated to dryness under reduced pressure to obtain 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propan-1-ol (0.23 g) as white powder.
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-703fbf2958744f0ea467833afb1d0b3b |
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| Source note | uspto-grants-2011_12 |
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