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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350040Generated: October 30, 2026

Potassium Carbonate → HCID 69421552, compound

https://huagongshe.com/reaction/350040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantEthyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionateHCID 23024736—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69421552HCID 6942155248%

Reaction Steps

A mixture of ethyl 3-[1-(4-hydroxybenzyl)-4-phenyl-3-pyrrolyl]propionate (1.35 g), 3-picolyl chloride hydrochloride (0.76 g), potassium carbonate (0.85 g) and N,N-dimethylformamide (15 ml) was stirred at room temperature overnight. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and then concentrated. The residue was subjected to silica gel column chromatography, and an oily substance was obtained from the fraction eluted with ethyl acetate-hexane (1:1, volume ratio). A mixture of the oily substance obtained, 1N aqueous sodium hydroxide solution (8 ml), tetrahydrofuran (8 ml) and ethanol (8 ml) was stirred at room temperature for 3 hours and the organic solvent was removed under reduced pressure. After adding water, the residue was neutralized by adding 1N hydrochloric acid. The colorless crystals obtained were collected by filtration to yield 3-[4-phenyl-1-[4-(3-pyridylmethoxy)benzyl]-3-pyrrolyl]propionic acid (0.76 g, yield: 48%). This was recrystallized from ethanol-water. Melting point: 131–132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-2c20326dda904fd08357c90b5c390faf
Source noteuspto-grants-2007_02