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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406691Generated: October 31, 2026

2-Acetylthiophene → HCID 51353026, compound

https://huagongshe.com/reaction/1406691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylthiopheneHCID 6920—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 1515983HCID 1515983—
SolventEthanolHCID 702—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 51353026HCID 5135302670%

Reaction Conditions

Temperature27 °C

Reaction Steps

To a stirred solution of 2-acetyl thiophene (126 mg, 1.0 mmol) and a 6-(4-methoxyphenyl) imidazo[2,1-b]thiazol-5-carbaldehyde (258 mg, 1.0 mmol) in ethanol (20 ml) 10% aqueous solution of NaOH was added (5 ml). The reaction mixture was stirred at room temperature 27° C. for 4 h and the reaction was monitored by TLC using ethyl acetate-hexane (3:7) as a solvent system. The solvent was evaporated under vacuum then the residue was dissolved in ethylacetate/water. The organic layer was washed with brine and evaporated. This was further purified by column chromatography using ethyl acetate:hexane (2:8) as a solvent system to obtain the pure product (16a) as yellow solid (256 mg, 70% yield). Mp: 169-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916711B2
Source datasetuspto-grants-2014_12
ORD IDord-ace7ed4d81764ab283b99338ad1b0108
Source noteuspto-grants-2014_12