HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896755Generated: November 1, 2026
5-Methyl-2-thiophenecarboxaldehyde → HCID 67331876, compound
https://huagongshe.com/reaction/1896755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Methyl-2-thiophenecarboxaldehyde | HCID 61663 | — |
| Reactant | 2-Amino-4-(ethylsulphonyl)phenol | HCID 643218 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67331876 | HCID 67331876 | 0.3% |
Reaction Steps
To a stirred solution of 2-amino-4-(ethylsulfonyl)phenol (452.7 mg, 2.25 mmol) in ethanol (17 mL) was added 5-methyl-2-thiophenecarboxaldehyde (242 μL, 2.25 mmol). The mixture was heated at 70° C. for 70 min. After cooling, a small amount of precipitate was formed. After filtration and evaporation of the filtrate, the resulting product was dissolved in acetonitrile (9.8 mL) and lead tetraacetate (887 mg, 2 mmol) was added. The resulting mixture was heated at 100° C. for 5 min. After cooling, the reaction mixture was filtered off, and the filtrate evaporated in vacuo. The resulting mixture was purified by column chromatography eluting with ethyl acetate/hexanes 20:80 v/v, and then purified by reverse phase HPLC to afford 2.2 mg (0.3%) of the title product (LCMS RT=6.41 min, MH+ 308.1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518980B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-68a2bd8ab47f42b9bfd7c00577bba2fe |
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| Source note | uspto-grants-2013_08 |
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