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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1450442Erstellt: 26. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzo(B)ThiopheneHCID 7221—
Edukt1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinecarboxylic acid, methyl esterHCID 10869587—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-(benzo[b]thiophene-2-yl)-2-benzo[b]thiophenemethanolHCID 18930359—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05602147
Quelldatensatzuspto-grants-1997_02
ORD IDord-63c5ab7c8d7743c2856cab6293760712
Quellennotizuspto-grants-1997_02