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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829Generated: October 26, 2026

Cesium carbonate → Methyl 3-(3-acetamidophenoxymethyl)-2-thiophenecarboxylate

https://huagongshe.com/reaction/1829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-HydroxyacetanilideHCID 12124—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-(bromomethyl)thiophene-2-carboxylateHCID 10537693—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(3-acetamidophenoxymethyl)-2-thiophenecarboxylateHCID 1969307275.1%

Reaction Steps

To a solution of 3-acetamidophenol (4.79 g, 31.7 mmol) in dimethylformamide (50 ml) was added cesium carbonate (5.67 g, 17.4 mmol), followed by stirring at room temperature for 30 minutes. To the resulting mixture was added methyl 3-bromomethyl-2-thiophenecarboxylate (8.94 g, 38.0 mmol), and the mixture was stirred overnight at room temperature. After the reaction was completed, the reaction mixture was poured into a 5% aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the organic layer was concentrated under reduced pressure. The obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=5/1), followed by trituration with hexane to give methyl 3-(3-acetamidophenoxymethyl)-2-thiophenecarboxylate as a white solid (7.27 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726325
Source datasetuspto-grants-1998_03
ORD IDord-29f57c2dee5f49d5a4d2fd451c9a7d4b
Source noteuspto-grants-1998_03