HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42782Generated: October 30, 2026
Ethylene Glycol → 2-Bromo-6-(2-methyl-1,3-dioxolan-2-yl)pyridine
https://huagongshe.com/reaction/42782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Acetyl-6-bromopyridine | HCID 11298578 | — |
| Product | 2-Bromo-6-(2-methyl-1,3-dioxolan-2-yl)pyridine | HCID 12164282 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(6-bromo-pyridin-2-yl)-ethanone (1880 mg, 9.40 mmol) in ethylene glycol (10.00 mL, 179.32 mmol) was treated with trimethylorthoformate (2.10 mL, 19.16 mmol) followed by LiBF4 (180 mg, 1.88 mmol). The reaction mixture was heated at 95° C. for 5 h. Sat. aq. Na2CO3 was added and the mixture was extracted twice with ether and the combined organic extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (50:50 hept-EA)=0.57.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536209B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-886bb6659579497e863c091669bff0b7 |
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| Source note | uspto-grants-2013_09 |
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