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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910276Generated: October 28, 2026

Potassium Carbonate → N-[4-(4-formylphenyl)thiophen-2-ylmethyl]-N-methylbenzamide

https://huagongshe.com/reaction/910276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
ReactantN-[(4-Bromo-2-thienyl)methyl]-N-methylbenzamideHCID 47042144—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
ProductN-[4-(4-formylphenyl)thiophen-2-ylmethyl]-N-methylbenzamideHCID 8601744479.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

3 g (20 mmol) of 4-formylbenzeneboronic acid are added to a solution of 4.75 g (15 mmol) of N-(4-bromothiophen-2-ylmethyl) -N-methylbenzamide in 60 ml of toluene, followed by dropwise addition of 5.5 g (40 mmol) of aqueous potassium carbonate solution. The reaction medium is degassed, 530 mg (0.5 mmol) of tetrakis (triphenylphosphine) palladium are then added and the medium is heated at 80° C. for 18 hours. After extraction with ethyl acetate and washing with water, the organic phase is dried over magnesium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with a 1/1 heptane/ethyl acetate mixture. 4 g (78%) of N-[4-(4-formylphenyl)thiophen-2-ylmethyl]-N-methyl-benzamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022079B2
Source datasetuspto-grants-2011_09
ORD IDord-a329dfe6b0024417a6256a079ad19f82
Source noteuspto-grants-2011_09