HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 2-methylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylthiophene-3-carboxylic acid | HCID 4625409 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 2-methylthiophene-3-carboxylate | HCID 13133923 | — |
Reaction Steps
To a solution of 3.30 g (23.2 mmol) of 2-methyl-3-thiophenecarboxylic acid in 100 ml of acetone was added 16.04 g (116.1 mmol) of anhydrous potassium carbonate and 16.47 g (7.2 ml, 116.1 mmol) of methyl iodide. The reaction mixture was allowed to stir at room temperature for 20.25 hours. A white precipitate formed. The white precipitate was filtered, washed with ethyl ether and discarded. The filtrate was concentrated in vacuo, partitioned between 250 ml of water and 250 ml of pentane and the layers separated. The organic phase was washed with a saturated solution of Na2 SO3, dried over Na2SO4, filtered and concentrated by rotary evaporation to give the title compound as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05677320 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-3d98ed0abd3f4678b99ceb8400ec6807 |
| Source note | uspto-grants-1997_10 |