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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(b)thiophene, 3-bromo-HCID 123250—
ReactantHCID 15681286HCID 15681286—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 18930336HCID 18930336—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541200
Source datasetuspto-grants-1996_07
ORD IDord-9dac50c1e8a341a1b7c04c725be68a82
Source noteuspto-grants-1996_07