HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736445Generated: October 29, 2026
Benzo(b)thiophene, 3-bromo- → HCID 18930336, compound
https://huagongshe.com/reaction/1736445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzo(b)thiophene, 3-bromo- | HCID 123250 | — |
| Reactant | HCID 15681286 | HCID 15681286 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 18930336 | HCID 18930336 | — |
Reaction Steps
Dissolve n-butyllithium (9.4 mL of a 2.5M solution in hexane, 23.46 mmol) in anhydrous ethyl ether (100 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, a solution of 3-bromobenzo[b]thiophene (5.0 g, 23.46 mmol) in anhydrous ethyl ether (50 mL). Stir at -78° C. for 30 minutes then add, by dropwise addition, a solution of 1-(2-phenylethyl)-4-piperidinecarboxaldehyde (5.10 g, 23.46 mmol) in anhydrous ethyl ether (50 mL). Stir for 5 hours at -78° C., remove the ice bath and stir for an additional 1 hour. Quench with saturated ammonium chloride (150 mL) and stir overnight. Separate the organic phase and extract the aqueous phase with ethyl ether and methylene chloride. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by recrystallization (isopropanol) to give the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05541200 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-9dac50c1e8a341a1b7c04c725be68a82 |
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| Source note | uspto-grants-1996_07 |
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