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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068663Generated: November 1, 2026

Formamide → 5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/2068663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantSulfuric AcidHCID 1118—
Reactant5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl esterHCID 53904546—
Product5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl esterHCID 58110244—

Reaction Conditions

Temperature150 °C

Reaction Steps

5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester (0.60 g, 2.28 mmol) was suspended in formamide (10 mL) then sulfuric acid (1 mL) was added and the tube purged with nitrogen then sealed. The mixture was heated at 150° C. by microwave irradiation for 15 minutes. The resultant solution was diluted with HCl (1 N) and water and extracted with ethyl acetate (×3). The organic phase was dried over sodium sulfate and evaporated then purified by chromatography on a silica II cartridge, eluting with 1:1 DCM: cyclohexane to afford 5-oxazol-4-yl-thiophene-3-carboxylic acid methyl ester as a pale yellow solid (0.197 g). LCMS m/z 210.14 [M+H]+ R.T.=3.64 min (Analytical Method 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299063B2
Source datasetuspto-grants-2012_10
ORD IDord-86a16e5b593a4773ba165b03cd688d61
Source noteuspto-grants-2012_10