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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927646Generated: October 31, 2026

Potassium Carbonate → 2-{4-[2-(1,3-Dioxolan-2-yl)vinyl]-phenyl)pyridine

https://huagongshe.com/reaction/1927646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant4-Pyridin-2-ylbenzaldehydeHCID 1515240—
Reactant(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromideHCID 2724194—
SolventDichloromethaneHCID 6344—
Product2-{4-[2-(1,3-Dioxolan-2-yl)vinyl]-phenyl)pyridineHCID 68673097—

Reaction Steps

A mixture of 4-(2-pyridyl)benzaldehyde (6.0 g, 32.8 mmol), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (18.3 g, 42.6 mmol), tris[2-(2-methoxyethoxy)ethyl]amine (13.76 g, 42.6 mmol), dichloromethane (200 mL) and saturated potassium carbonate (200 mL) was heated to reflux overnight. The reaction was cooled to rt and the product was extracted with ethyl acetate-hexanes (2×). The extracts were washed with water and brine, and concentrated to afford 2-{4-[2-(1,3-dioxolan-2-yl)vinyl]-phenyl)pyridine, which was dissolved in methanol (120 mL) and was stirred with Pd on carbon (10%, 1.75 g) under 1 atmosphere of hydrogen overnight. The reaction mixture was filtered through Celite, and the filtrate was concentrated to afford crude 2-{4-[2-(1,3-dioxolan-2-yl)ethyl]phenyl}pyridine, which was dissolved in acetone (80 mL) and treated with 4 M HCl (aq., 80 mL). After stirring at rt for 20 h, the product was extracted with ethyl acetate-hexanes (2×). The extracts were washed with water and brine, and concentrated, and the residue was purified on silica gel eluted with a 5-100% ethyl acetate in hexanes to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183275B2
Source datasetuspto-grants-2012_05
ORD IDord-378a1c44cd5a4517aa4ba4a7fa44f3ad
Source noteuspto-grants-2012_05