HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437141Generated: November 1, 2026
3-Thiophencarboxamide,N-methyl- → HCID 10244631, compound
https://huagongshe.com/reaction/1437141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Thiophencarboxamide,N-methyl- | HCID 819553 | — |
| Reactant | 2,2,2-Trifluoro-N-(hydroxymethyl)acetamide | HCID 3084931 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 10244631 | HCID 10244631 | — |
Reaction Steps
To suspension of N-methyl-3-thiophenecarboxamide (1.12 g) (prepared according to J. Org. Chem. (1976), 41(23), 3668-74) in concentrated aqueous sulphuric acid (25 ml) at 0-5° C. was added N-(hydroxymethyl)trifluoroacetamide (1.134 g). The suspension was allowed to warm to 20° C. and stirred for 2 h. The mixture was poured onto ice (150 g) and diluted with ethyl acetate (200 ml). The biphase mixture was diluted with saturated sodium hydrogen carbonate (200 ml) and treated with sodium hydrogen carbonate (21 g). The phases were separated and the organic phase washed with saturated sodium hydrogen carbonate (150 ml×2). The combined aqueous phases were extracted with ethyl acetate (100 ml). The combined organic extracts were concentrated in vacuo. The residue was pre-absorbed onto silica and purified by biotage (90 g) eluting with 1:1 to 0:1 cyclohexane:ethyl acetate to give the title compound as a white solid (0.7129).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622464B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-be5173694d8d4c139d62c84e87399bc1 |
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| Source note | uspto-grants-2009_11 |
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