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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914569Generated: October 25, 2026

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

https://huagongshe.com/reaction/1914569

Reaction equation

Participants

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

Reaction Conditions

Temperature170 °C

Reaction Steps

5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester (0.4 g, 1.52 mmol) was dissolved in formamide (2 mL) and the tube purged with nitrogen and then sealed. The mixture was heated at 170° C. for 20 minutes. The resultant solution was diluted with HCl (1 M) and water and washed with ethyl acetate. The organic phase was evaporated then purified by chromatography on a silica II cartridge, eluting with 2:1 pentane:DCM to neat DCM, to give the side product, 5-oxazol-4-yl-thiophene-3-carboxylic acid methyl ester as white solid (0.049 g). LCMS m/z 251.35 [M+MeCN+H]+ R. T.=3.07 min (Analytical Method 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614209B2
Source datasetuspto-grants-2013_12
ORD IDord-b807fab4938e4987a356bb06be0a6677
Source noteuspto-grants-2013_12