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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489101Generated: October 31, 2026

Methyl iodide → Methyl 2-methylthiophene-3-carboxylate

https://huagongshe.com/reaction/1489101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methylthiophene-3-carboxylic acidHCID 4625409—
SolventAcetoneHCID 180—
ProductMethyl 2-methylthiophene-3-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677320
Source datasetuspto-grants-1997_10
ORD IDord-3d98ed0abd3f4678b99ceb8400ec6807
Source noteuspto-grants-1997_10