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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | N-[(4-Bromo-2-thienyl)methyl]-N-methylbenzamide | HCID 47042144 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[4-(4-formylphenyl)thiophen-2-ylmethyl]-N-methylbenzamide | HCID 86017444 | 79.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022079B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a329dfe6b0024417a6256a079ad19f82 |
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| Source note | uspto-grants-2011_09 |
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