Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886923Generated: November 1, 2026

5-Methyl-2-thiophenecarboxaldehyde → HCID 67331876, compound

https://huagongshe.com/reaction/1886923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-2-thiophenecarboxaldehydeHCID 61663—
Reactant2-Amino-4-(ethylsulphonyl)phenolHCID 643218—
ReactantHCID 178418268HCID 178418268—
SolventEthanolHCID 702—
ProductHCID 67331876HCID 673318760.3%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501713B2
Source datasetuspto-grants-2013_08
ORD IDord-66241ae8206d4da2909d366e792ddb9c
Source noteuspto-grants-2013_08