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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789210Generated: October 26, 2026

Potassium Carbonate → 8-(Acetoxymethyl)-3-phenylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1789210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-2-phenylacetaldehydeHCID 10888901—
Reactant3-(Acetoxymethyl)-2-pyridinamineHCID 20188855—
SolventWaterHCID 962—
Product8-(Acetoxymethyl)-3-phenylimidazo[1,2-a]pyridineHCID 2018884659.2%

Reaction Steps

A mixture of 4.4 g (26 mmole) of 3-(acetoxymethyl)-2-pyridinamine and 6.0 g (30 mmole) of 2-bromo-2-phenylacetaldehyde was heated at 65°. The mixture was dissolved in water, made basic with aqueous potassium carbonate, and extracted with dichloromethane. The organic layer was washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with diethyl ether to yield 4.1 g of 8-(acetoxymethyl)-3-phenylimidazo[1,2-a]pyridine as confirmed by the nmr and infrared spectra and by elemental analysis. [Calcd. for C16H14N2O2 : C, 72.17; H, 5.30; N, 10.52. Found: C, 71.90; H, 5.25; N, 10.43.] The title compound (1.5 g) was prepared by the method described in Example 26 using 1.3 g (5 mmole) of 8-(acetoxymethyl)-3-phenylimidazo[1,2-a]pyridine instead of 8-hydroxymethyl-2-phenylimidazo[1,2-a]pyridine. Structure assignment was supported by the nmr and infrared spectra and by elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04687775
Source datasetuspto-grants-1987_08
ORD IDord-ec4b142bf5f74761be211a314d93711e
Source noteuspto-grants-1987_08