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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256703생성일: 2026년 10월 27일

Hydrochloric Acid → 4'-Vinyl-3-hydroxyflavone

https://huagongshe.com/reaction/256703

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Hydrogen PeroxideHCID 784—
반응물4-VinylbenzaldehydeHCID 39389—
반응물alpha-HydroxyacetophenoneHCID 68490—
용매EthanolHCID 702—
용매Sodium HydroxideHCID 14798—
생성물4'-Vinyl-3-hydroxyflavoneHCID 10901472—

반응 단계

13 gms of 4-vinyl benzaldehyde 0.955 moles) was added to a flask containing 13.9 gms of 2-hydroxyacetophenone (0.955) in 150 ml alcohol. In a separate RB flask, 13 gms of NaOH was dissolved in 100 ml of aqueous ethyl alcohol (75%). The NaOH solution was added to the reaction mixture at once. The color of the solution immediately changed from colorless to yellow to pink, and then, finally, to a dark red precipitate. The solution was allowed to sit at room temperature overnight. The next morning, 6 gms of NaOH in 200 ml of aqueous ethyl alcohol (75%) was added to the Precipitate and the reaction mixture was cooled in an icebath for 15 mins. In a separate RB flask, a solution of 50 ml of 30% hydrogen peroxide solution in 50 ml of aqueous ethyl alcohol (75%) was added to the reaction flask at once at 0°-5° C. The red colored precipitate dissolved immediately and the color of the solution slowly changed from red to yellow. The solution was gradually warmed to room temperature and was stirred for 6 hrs. The reaction mixture was neutralized with dil. HCl at 0°-4° C. A white precipitate formed and was filtered and washed with distilled water until it was free from acid. The color of the product slowly changed from colorless to light pink or to light brown during filtration.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258478
출처 데이터셋uspto-grants-1993_11
ORD IDord-89fea78c44404c0f9bc363f38ceeabe5
출처 메모uspto-grants-1993_11