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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium CarbonateHCID 10340—
Reactant2-Acetyl-6-bromopyridineHCID 11298578—
Product2-Bromo-6-(2-methyl-1,3-dioxolan-2-yl)pyridineHCID 12164282—

Reaction Conditions

Temperature95 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-886bb6659579497e863c091669bff0b7
Source noteuspto-grants-2013_09