HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916206Generated: November 2, 2026
Water → 3-(4-Benzo[b]thiophen-4-yl-piperazin-1-yl)propanol
https://huagongshe.com/reaction/1916206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| 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 | Tetrahydrofuran | HCID 8028 | — |
| 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 tetrahydrofuran (55 ml) with cooling in an ice-bath, followed by stirring at room temperature for 4 hours. Water (1.2 ml), 15% sodium hydroxide aqueous solution (1.2 ml), and water (3.6 ml) were added to the reaction mixture in this order with stirring at room temperature. Insoluble matters were removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→ethyl acetate), then concentrated and dried under reduced pressure to obtain 3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propane-1-ol (0.23 g) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618109B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d670cde82e9c4ddfbd33dc802ae5d14c |
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| Source note | uspto-grants-2013_12 |
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