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HRID 647894作成日:2026年10月25日

Sodium Iodide → 5-(2-Formyl-3-methoxyphenoxy)pentanoic acid

https://huagongshe.com/reaction/647894

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Potassium CarbonateHCID 11430—
反応物6-MethoxysalicylaldehydeHCID 69692—
反応物Ethyl 5-bromovalerateHCID 84580—
溶媒EthanolHCID 702—
生成物5-(2-Formyl-3-methoxyphenoxy)pentanoic acidHCID 20484339—

反応手順

2-Hydroxy-6-methoxybenzaldehyde (16.875 g., 0.111 M), ethyl 5-bromopentanoate (23.25 g., 17.6 ml., 0.111 M), anhydrous potassium carbonate (16.5 g.), sodium iodide (0.675 g.) and 95% ethanol (150 ml.) were refluxed with stirring (16 hrs). 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 and water. The ethereal layer was separated and washed with 2 N sodium hydroxide solution, water, dried (sodium sulphate) and evaporated. The residue was dissolved in 95% ethanol (300 ml.) and 0.66 N sodium hydroxide solution (450 ml.) and stirred at ambient temperature (4 hrs). The reaction mixture was evaporated to half volume and diluted with water. The mixture was extracted once with ether and the aqueous layer acidified with concentrated hydrochloric acid with cooling. The crystalline solid formed was filtered off and washed well with water. Recrystallisation from ethyl acetate-petrol gave 5-(2-formyl-3-methoxyphenoxy)pentanoic acid, m.p. 99°-101° C. (Found: C, 61.98; H, 6.58. C13H16O5 requires C, 61.89; H, 6.39%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04410537
出典データセットuspto-grants-1983_10
ORD IDord-b9e9f61a990a43eeb95ac4522d7ce523
出典メモuspto-grants-1983_10