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HRID 26218생성일: 2026년 10월 26일

1,2-Epoxybutane → 6-Carboxy2'-(2-hydroxy-butoxy)-flavone

https://huagongshe.com/reaction/26218

반응식

참여 물질

역할이름HCID투입량
반응물1,2-EpoxybutaneHCID 7834—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물6-Carbomethoxy-2'-hydroxy-flavoneHCID 12407866—
용매1,4-DioxaneHCID 31275—
생성물6-Carboxy2'-(2-hydroxy-butoxy)-flavoneHCID 2132501639.3%

반응 단계

A mixture consisting of 6-carbomethoxy-2'-hydroxy-flavone (10 g), obtained according to the method described in Example 2, and 1,2-epoxy-butane (6 g) and benzyl-trimethylammonium hydroxide (0.5 ml) in dioxane (40 ml) was kept at reflux temperature for 48 hours. After cooling, dilution with water, and extraction with ethylacetate, the organic phase was washed with potassium carbonate 5% and water. The solution was evaporated to dryness, and the resulting product was treated with the stoichiometric quantity of a solution of potassium hydroxide 1% in ethanol 95% at reflux temperature for an hour. After acidification with acetic acid, concentration under vacuum, dilution with water, filtration and double crystallisation from ethanol, 6-carboxy2'-(2-hydroxy-butoxy)-flavone (4.7 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148900
출처 데이터셋uspto-grants-1979_04
ORD IDord-8698bf11a6e24a6491845b020b8dccb2
출처 메모uspto-grants-1979_04