HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78071Generated: October 25, 2026
Dimethylformamide → 3-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)-benzaldehyde
https://huagongshe.com/reaction/78071
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Reactant | (5-Fluoropyridin-2-yl)methanol | HCID 24729312 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)-benzaldehyde | HCID 59255474 | 42.2% |
Reaction Steps
To an N,N-dimethylformamide (20.0 mL) solution of (5-fluoro-pyridin-2-yl)-methanol (760 mg, 5.98 mmol) described in Manufacturing Example 41-1-1 was added sodium hydride (239 mg, 5.98 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 10 minutes at room temperature. 3,4-Difluorobenzaldehyde (935 mg, 6.58 mmol) was then added at room temperature, and stirred for 30 minutes at room temperature. 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=1:3) to obtain the title compound (629 mg, 42.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841327B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6bbc91011dee41c3900085ff4d95ec9c |
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| Source note | uspto-grants-2014_09 |
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