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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133546Erstellt: 24. Oktober 2026

Sodium Carbonate → N-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamide

https://huagongshe.com/de/reaction/133546

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktPhenylboronic AcidHCID 66827—
EduktN-(3-benzoyl-5-bromo-thiophen-2-yl) acetamideHCID 16640231—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
ProduktN-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamideHCID 6889539088,6%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A stirred solution of 0.448 g (1.38 mmol) of N-(3-benzoyl-5-bromo-thiophen-2-yl) acetamide in 20 ml toluene and 10 ml EtOH was degassed with argon. Tetrakis-(triphenylphosphine) palladium (0) (0.320 g, 0.27 mmol), phenyl boronic acid (0.194 g, 1.59 mmol) and 20 ml of an aqueous solution of Na2CO3 1N were added. The mixture was heated at 90° C. for 1 hour before cooling down to RT, filtered through Celite and concentrated. The mixture was extracted with ethyl acetate and aq. NaHCO3. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 6:1) afforded 0.393 g (88%) N-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamide as a light yellow solid. ES-MS m/e (%): 322 (M+H+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390903B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-05943aea103c471bbd9ee1e2aee9c135
Quellennotizuspto-grants-2008_06