HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693994Generated: October 26, 2026
Dimethylformamide → 4-(2-Fluorophenoxy)benzaldehyde
https://huagongshe.com/reaction/1693994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Fluorophenol | HCID 9707 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Fluorophenoxy)benzaldehyde | HCID 10798745 | 99.4% |
Reaction Steps
To an N,N-dimethylformamide (30.0 mL) solution of 2-fluorophenol (5.43 g, 48.4 mmol) and 4-fluorobenzaldehyde (3.00 g, 24.2 mmol) was added potassium carbonate (10.1 g, 72.5 mmol) under nitrogen atmosphere, which was stirred for 16 hours at 80° C. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15→1:10) to obtain the title compound (5.20 g, 99.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158657B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-8626a3d2a0764489a3dc0fcc845dd8e6 |
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| Source note | uspto-grants-2012_04 |
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