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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420653Generated: October 31, 2026

Ethylene Glycol → HCID 44754838, compound

https://huagongshe.com/reaction/2420653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Bromopyridine-2-carbaldehydeHCID 9877562—
SolventTolueneHCID 1140—
ProductHCID 44754838HCID 4475483884%

Reaction Steps

Ethyleneglycol (14.88 g, 0.24 mol) and p-toluenesulfonic acid (3 g, 0.16 mol) are added to a solution of 5-bromopyridine-2-carbaldehyde (30 g, 0.16 mol) in toluene (150 ml) at room temperature and the mixture is stirred for 10 hrs at refluxing temperature. After cooling to room temperature, the mixture is quenched with saturated aqueous NH4Cl, extracted with CH2Cl2 and washed with H2O. The aqueous layer is extracted with CH2Cl2 and the combined organic extract is washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (hexane-AcOEt (9:1 V/V)) to afford 5-bromo-2-(1,3-dioxolan-2-yl)pyridine (30.9 g, 84%) as a colorless oil. %). 1H NMR (400 MHz, CDCl3) δ 8.69 (s, 1H), 7.87 (m, 1H), 7.45 (m, 1H), 5.83 (s, 1H), 4.13 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07955720B2
Source datasetuspto-grants-2011_06
ORD IDord-f1d94a70a38a45f89e8192cf40767d5b
Source noteuspto-grants-2011_06