HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640361Generated: October 26, 2026
Dimethylformamide → 2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehyde
https://huagongshe.com/reaction/640361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Fluoro-4-hydroxybenzaldehyde | HCID 587246 | — |
| Reactant | 2-(Chloromethyl)-5-fluoropyridine | HCID 21698059 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehyde | HCID 59255356 | 42.2% |
Reaction Steps
To an N,N-dimethylformamide (20.0 mL) solution of 2-fluoro-4-hydroxy-benzaldehyde (1.48 g, 10.2 mmol) was added sodium hydride (411 mg, 10.3 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 20 minutes at room temperature. 2-Chloromethyl-5-fluoro-pyridine (1.20 g, 8.56 mmol) described in Manufacturing Example 41-1-2 was then added at room temperature, and stirred for 30 minutes at 80° C. Water was added at room temperature to the reaction solution, 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=1:5→1:2) to obtain the title compound (901 mg, 42.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691882B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-509b35bb32cb415187b898623294edf1 |
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| Source note | uspto-grants-2010_04 |
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