HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446449Generated: October 27, 2026
3-Ethoxy-4-fluorobenzaldehyde → 3-ethoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde
https://huagongshe.com/reaction/1446449
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Ethoxy-4-fluorobenzaldehyde | HCID 42614294 | — |
| Reactant | HCID 178418800 | HCID 178418800 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-ethoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde | HCID 73014041 | 18% |
Reaction Steps
4-methylimidazole (244 mg) was added to a DMF (3 mL) solution of 3-ethoxy-4-fluorobenzaldehyde (250 mg) obtained above, and the reaction solution was agitated at 150° C. for 4 hours. The reaction solution was concentrated as it was after the reaction ended, water and ethyl acetate were added to the obtained reaction residue, and the organic layer was separated. The obtained organic layer was washed with a saturated sodium chloride solution, and the solvent was evaporated under reduced pressure after dried over anhydrous magnesium sulfate. The obtained residue was purified by silica gel column chromatography (elution solvent:heptane-ethyl acetate 1:4), and 60 mg (18%) of 3-ethoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde was obtained. The physical properties of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07667041B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-a0b39bdf62724bbeb6c6f2ac0825a32b |
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| Source note | uspto-grants-2010_02 |
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