HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394147Generated: October 31, 2026
4-Fluorophenol → 4-(4-Fluorophenoxy)benzaldehyde
https://huagongshe.com/reaction/1394147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Fluorophenoxy)benzaldehyde | HCID 3856802 | — |
Reaction Steps
To a solution of 4-fluorophenol (1.06 g) in anhydrous DMF (10 mL) were added anhydrous potassium carbonate (2.07 g) and 4-fluorobenzaldehyde (1.2 g) at room temperature. The reaction was stirred at 100° C. for 16 h, then cooled to room temperature and diluted with ether. The organic layer was washed with 1N sodium hydroxide, and then with water, dried over sodium sulphate, and concentrated under reduced pressure. The crude aldehyde obtained was purified by flash-column chromatography on silica-gel using 20% EtOAc in hexanes to provide the pure aldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348348B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-4b777751155f492480087b5dd69aa19e |
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| Source note | uspto-grants-2008_03 |
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