HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81639Generated: October 25, 2026
Dimethylformamide → 5-[2-(1,3-Dioxolan-2-yl)ethoxy]-2,3-difluoropyridine
https://huagongshe.com/reaction/81639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(2-Bromoethyl)-1,3-dioxolane | HCID 87776 | — |
| Reactant | 5,6-Difluoropyridin-3-ol | HCID 68430860 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[2-(1,3-Dioxolan-2-yl)ethoxy]-2,3-difluoropyridine | HCID 68429762 | 38.1% |
Reaction Steps
Cesium carbonate (33 g, 100 mmol) and 2-(2-bromoethyl)-1,3-dioxolane (12 g, 67 mmol) were added to an N,N-dimethylformamide suspension (30 ml) of 5,6-difluoropyridin-3-ol (8.8 g, 67 mmol), and stirred at 100° C. for 1 hour. The reaction solution was cooled to room temperature, water was added, and extracted with ethyl acetate. The organic layer was washed with saturated saline water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:chloroform=1:1 to 0:1) to obtain 5-[2-(1,3-dioxolan-2-yl)ethoxy]-2,3-difluoropyridine (5.9 g, yield: 38%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846700B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-9e72d3e1c42543f1aabdb607ad88b529 |
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| Source note | uspto-grants-2014_09 |
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