HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068634Generated: October 25, 2026
Formamide → 5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester
https://huagongshe.com/reaction/2068634
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamide | HCID 713 | — |
| Reactant | 5-(2-Bromo-acetyl)-thiophene-3-carboxylic acid methyl ester | HCID 53904546 | — |
| Product | 5-Oxazol-4-yl-thiophene-3-carboxylic acid methyl ester | HCID 58110244 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299063B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-30f48cd78caf41b1b6162ee6901eeea9 |
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| Source note | uspto-grants-2012_10 |
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