돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647894생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/647894

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물6-MethoxysalicylaldehydeHCID 69692—
반응물Ethyl 5-bromovalerateHCID 84580—
용매EthanolHCID 702—
생성물5-(2-Formyl-3-methoxyphenoxy)pentanoic acidHCID 20484339—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04410537
출처 데이터셋uspto-grants-1983_10
ORD IDord-b9e9f61a990a43eeb95ac4522d7ce523
출처 메모uspto-grants-1983_10