HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640440Generated: October 29, 2026
Dimethylformamide → 5-[1,3]Dioxolan-2-yl-2-(pyridin-2-yloxymethyl)-pyridine
https://huagongshe.com/reaction/640440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Fluoropyridine | HCID 9746 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (5-[1,3]Dioxolan-2-yl-pyridin-2-yl)-methanol | HCID 59255267 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[1,3]Dioxolan-2-yl-2-(pyridin-2-yloxymethyl)-pyridine | HCID 59255338 | 77.3% |
Reaction Steps
To an N,N-dimethylformamide (40 mL) solution of (5-[1,3]dioxolan-2-yl-pyridin-2-yl)-methanol (1.37 g, 7.56 mmol) described in Manufacturing Example 154-1-4 was added sodium hydride (333 mg, 8.32 mmol, 60% in oil), which was stirred for 5 minutes at 0° C. Next, 2-fluoropyridine (716 μL, 8.32 mmol) was added to the reaction mixture, which was stirred for 45 minutes at 50° C. Water was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1 to 1:1) to obtain the title compound (1.51 g, 77%).
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-5a19e8e7577745ae87b0565ac7eb0d23 |
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| Source note | uspto-grants-2010_04 |
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