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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406690Generated: November 1, 2026

2-Acetylnaphthalene → HCID 51352711, compound

https://huagongshe.com/reaction/1406690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylnaphthaleneHCID 7122—
ReactantSodium HydroxideHCID 14798—
Reactant6-(4-Fluorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehydeHCID 2759102—
SolventEthanolHCID 702—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 51352711HCID 5135271175%

Reaction Conditions

Temperature27 °C

Reaction Steps

To a stirred solution of 2-acetyl napthalene (170 mg, 1.0 mmol) and a 6-(4-fluorophenyl) imidazo[2,1-b]thiazol-5-carbaldehyde (246 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 (12e) as yellow solid (298 mg, 75% yield). Mp: 216-218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916711B2
Source datasetuspto-grants-2014_12
ORD IDord-80a3e0e1c9af4876bde65de86e5a53c2
Source noteuspto-grants-2014_12