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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35276Generated: October 26, 2026

Potassium Iodide → 4-Phenoxyphenoxyacetaldehyde diethyl acetal

https://huagongshe.com/reaction/35276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-PhenoxyphenolHCID 13254—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventDimethylformamideHCID 6228—
Product4-Phenoxyphenoxyacetaldehyde diethyl acetalHCID 13771703—

Reaction Conditions

Temperature150 °C

Reaction Steps

150 g of potassium carbonate and 4 g of finely powdered potassium iodide are added to a solution of 112 g (0.6 mole) of 4-phenoxyphenol and 157.6 g (0.8 mole) of bromoacetaldehyde diethyl acetal in 480 ml of dimethylformamide, and the batch is heated, under nitrogen, for 14 hours at 150° C. The salts are then removed by filtration from the reaction solution, and most of the dimethylformamide is distilled off in a water jet vacuum. The residue is dissolved in ether and the resultant solution is washed twice with water, three times with 20% potassium hydroxide solution and again with water. The ethereal solution is then dried over sodium sulfate and the ether is distilled off entirely. The resultant 4-phenoxyphenoxyacetaldehyde diethyl acetal is used without further purification for the preparation of the free aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766152
Source datasetuspto-grants-1988_08
ORD IDord-4d3ab34c7ec543f8a4e739c64817eae9
Source noteuspto-grants-1988_08