HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456553Generated: November 1, 2026
Hydrochloric Acid → 4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidine
https://huagongshe.com/reaction/456553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanone | HCID 23112505 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(7-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperidine | HCID 17952133 | 94.1% |
Reaction Steps
A mixture of 1-[4-(7-trifluoromethyl-benzo[b]thiophen-3-yl)-piperidin-1-yl]-ethanone (2.95 g, 9.01 mmol), concentrated HCl (30 mL), and ethanol was heated at 80° C. for 18 h. After cooling to room temperature, the reaction was basified with 20% aqueous potassium carbonate (150 mL) and the mixture extracted with DCM (2×100 mL). The organics were washed with water (100 mL), dried over potassium carbonate, filtered, and concentrated to give 2.42 g (94%) the desired product as an amber waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186724B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-28c8fff526aa4b68ab572e7e3fca8d4c |
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| Source note | uspto-grants-2007_03 |
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