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HRID 35276作成日:2026年10月24日

Potassium Iodide → 4-Phenoxyphenoxyacetaldehyde diethyl acetal

https://huagongshe.com/ja/reaction/35276

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物4-PhenoxyphenolHCID 13254—
反応物Ethane, 2-bromo-1,1-diethoxy-HCID 74852—
溶媒DimethylformamideHCID 6228—
生成物4-Phenoxyphenoxyacetaldehyde diethyl acetalHCID 13771703—

反応条件

温度150 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766152
出典データセットuspto-grants-1988_08
ORD IDord-4d3ab34c7ec543f8a4e739c64817eae9
出典メモuspto-grants-1988_08