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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377115Generated: October 26, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-

https://huagongshe.com/reaction/377115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant5-Ethyl-2-pyridineethanolHCID 78894—
CatalystBenzyltributylammonium chlorideHCID 159952—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzaldehyde, 4-[2-(5-ethyl-2-pyridinyl)ethoxy]-HCID 9881522114%

Reaction Steps

To a solution of sodium hydroxide (5 g) in water (30 ml), were added methylene chloride (100 ml), 5-ethyl-2-pyridineethanol (15 g) and benzyltributylammonium chloride (50% aqueous solution, 6 g), p-toluenesulfonyl chloride (23 g), and the mixture was stirred at room temperature for 2 hours. To the reaction mixture were added p-hydroxybenzaldehyde (12 g), water (100 ml) and sodium hydroxide (8 g) and the mixture was stirred at 40°-50° C. for 12 hours. The reaction mixture was separated into two phases and the methylene chloride layer was dried (MgSO4) and concentrated to give 28.6 g of crude 4-[2-(5-ethyl-2-pyridyl)ethoxy]benzaldehyde as oil. This oil was purified by silica gel chromatography to give 15.8 g (62%) of pure 4-[2-(5-ethyl-2-pyridyl)ethoxy]benzaldehyde as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036575
Source datasetuspto-grants-2000_02
ORD IDord-987d641a6d834cd5a8e3840d83e906e8
Source noteuspto-grants-2000_02