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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1491678Erstellt: 26. Oktober 2026

Trifluoroacetic acid → [Benzo[b]thiophene-3-yl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone

https://huagongshe.com/reaction/1491678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktPotassium CarbonateHCID 11430—
Edukt1-(2-Bromoethyl)-4-methoxybenzeneHCID 84427—
Edukt(Benzo[b]thiophene-3-yl)(4-piperidinyl)methanoneHCID 15337457—
LösungsmittelDimethylformamideHCID 6228—
Produkt[Benzo[b]thiophene-3-yl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanoneHCID 9799982—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Mix (benzo[b]thiophene-3-yl)(4-piperidinyl)methanone.CF3CO2H (2.0 g, 5.56 mmol), 2-(4-methoxyphenyl)ethyl bromide (1.27 g, 5.93 mmol ), potassium carbonate (1.95 g, 1.41 mmol) and anhydrous dimethylformamide (20 mL). Warm to approximately 90° C. and stir overnight. Allow to cool to room temperature and partition between a 2:1 mixture of ethyl acetate: toluene and water. Separate the aqueous phase and wash the organic phase with water and saturated sodium chloride. Dry (Na2SO4) and evaporate the solvent Purify by chromatography (40% ethyl acetate/hexane) and recrystallize (cyclohexane) to give the title compound pale yellow plates; mp 114°-116° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05371093
Quelldatensatzuspto-grants-1994_12
ORD IDord-889570dc210d4762a0c7ac4adf099917
Quellennotizuspto-grants-1994_12