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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133546Generated: October 25, 2026

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

https://huagongshe.com/reaction/133546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantN-(3-benzoyl-5-bromo-thiophen-2-yl) acetamideHCID 16640231—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamideHCID 6889539088.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390903B2
Source datasetuspto-grants-2008_06
ORD IDord-05943aea103c471bbd9ee1e2aee9c135
Source noteuspto-grants-2008_06