HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474596Generated: October 29, 2026
4-Fluorophenol → 4-(4-Fluorophenoxy)benzaldehyde
https://huagongshe.com/reaction/474596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Fluorophenoxy)benzaldehyde | HCID 3856802 | 84.3% |
Reaction Steps
To a solution of 4-fluorophenol (10 g, 89 mmol) and 4-fluorobenzaldehyde (11.07 g, 89 mmol) in DMF (200 mL) was added K2CO3 (13.33 g, 96 mmol). The mixture was heated at 140° C. for 4 h. After cooling to room temperature, the mixture was poured into of ice water (300 mL), and left stand overnight. The solid was collected by filtration, washed with water, re-dissolved in EA (200 mL) and washed with brine (100 mL). The organic phase was dried with sodium sulfate, filtered and concentrated to afford the title compound (17 g, 75 mmol, 84% yield) as yellow solid. LCMS: rt=1.52 min, [M+H+]=217
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637536B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-9810a23a9db841e2acc092dc3d1755a6 |
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| Source note | uspto-grants-2014_01 |
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