HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406690Generated: November 1, 2026
2-Acetylnaphthalene → HCID 51352711, compound
https://huagongshe.com/reaction/1406690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetylnaphthalene | HCID 7122 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(4-Fluorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde | HCID 2759102 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 51352711 | HCID 51352711 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916711B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-80a3e0e1c9af4876bde65de86e5a53c2 |
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| Source note | uspto-grants-2014_12 |
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