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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450442Generated: October 26, 2026

Benzo(B)Thiophene → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanol

https://huagongshe.com/reaction/1450442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
Reactant1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl esterHCID 10869587—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productalpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanolHCID 18930359—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve benzo[b]thiophene(10.0 g, 74.5 mmol) in anhydrous tetrahydrofuran (100 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, n-butyllithium (32.79 mL, 81.97 mmol) and stir briefly. Add, by dropwise addition, a solution of 1-[2-(4-methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl ester (20.67 g, 74.52 mmol) in anhydrous tetrahydrofuran (200 mL) and stir at -78° C. for 1.5 hours. Quench with saturated ammonium chloride, separate the organic phase and extract the aqueous phase with ethyl ether. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (50% ethyl acetate/hexane) and recrystallize (isopropanol) to give the title compound as a white solid; mp 168°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602147
Source datasetuspto-grants-1997_02
ORD IDord-63c5ab7c8d7743c2856cab6293760712
Source noteuspto-grants-1997_02