HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35276Generated: October 26, 2026
Potassium Iodide → 4-Phenoxyphenoxyacetaldehyde diethyl acetal
https://huagongshe.com/reaction/35276
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Phenoxyphenoxyacetaldehyde diethyl acetal | HCID 13771703 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766152 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-4d3ab34c7ec543f8a4e739c64817eae9 |
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| Source note | uspto-grants-1988_08 |
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