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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647900Generated: October 27, 2026

Potassium Carbonate → Ethyl 5-(2-formyl-3-methoxyphenoxy)pentanoate

https://huagongshe.com/reaction/647900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-MethoxysalicylaldehydeHCID 69692—
ReactantEthyl 5-bromovalerateHCID 84580—
CatalystSodium IodideHCID 5238—
SolventEthanolHCID 702—
ProductEthyl 5-(2-formyl-3-methoxyphenoxy)pentanoateHCID 2048434267%

Reaction Steps

2-Hydroxy-6-methoxybenzaldehyde (26.0 g, 0.17 M), ethyl 5-bromopentanoate (27.1 ml, 0.17 M), anhydrous potassium carbonate (25.4 g), sodium iodide (1.04 g) and ethanol (230 ml) were refluxed with stirring for 16 hours. The cooled reaction mixture was filtered and the solid washed well with ethanol. The filtrate was evaporated to dryness and the residue partitioned between ether (200 ml) and water (200 ml). The organic layer was separated and washed with 2 N sodium hydroxide solution (1×150 ml), water (1×150 ml), brine (1×150 ml), dried (magnesium sulphate) and evaporated to yield ethyl 5-(2-formyl-3-methoxyphenoxy)pentanoate 32.97 g, 67% yield, as a pale yellow oil that solidified on standing in the refrigerator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410537
Source datasetuspto-grants-1983_10
ORD IDord-d72cbaf0c69740f89ada3cd80373cf02
Source noteuspto-grants-1983_10