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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Thiophencarboxamide,N-methyl-HCID 819553—
Reactant2,2,2-Trifluoro-N-(hydroxymethyl)acetamideHCID 3084931—
SolventSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 10244631HCID 10244631—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622464B2
Source datasetuspto-grants-2009_11
ORD IDord-be5173694d8d4c139d62c84e87399bc1
Source noteuspto-grants-2009_11