HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561011Generated: October 26, 2026
Ethylene Glycol → 5-(1,3-Dioxolan-2-YL)-2-fluoropyridine
https://huagongshe.com/reaction/561011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Fluoro-5-formylpyridine | HCID 16414246 | — |
| Catalyst | Cupric chloride dihydrate | HCID 61482 | — |
| Solvent | Chloroform isopropyl alcohol | HCID 21906603 | — |
| Product | 5-(1,3-Dioxolan-2-YL)-2-fluoropyridine | HCID 60155792 | 39% |
Reaction Steps
In a pressure vessel, combine 6-fluoro-pyridine-3-carbaldehyde (4 g, 32 mmol), ethylene glycol (3 g, 48 mmol), copper (II) chloride di-hydrate (0.56 g, 3.2 mmol) and THF (10 mL). Heat the mixture at 100° C. for 1 hour. Dilute the mixture with chloroform-isopropanol (3:1, 100 mL). Wash the organic phase with saturated aqueous sodium chloride and water. Dry the organic layer over sodium sulfate. Concentrate the solution in vacuo to brown oil. Purify by column chromatography (20% ethyl acetate in hexane) to afford the title compound (2.1 g, 39%) as a pale yellow oil. MS (ES) m/z 170 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063212B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-f668c9cefe1e479794ff2c53df520d50 |
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| Source note | uspto-grants-2011_11 |
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