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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 623795생성일: 2026년 10월 24일

Benzaldehyde → Dalosirvat

https://huagongshe.com/ko/reaction/623795

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참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물TriethylamineHCID 8471—
반응물1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-(dimethylamino)propan-1-oneHCID 2825018—
촉매3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
용매1,4-DioxaneHCID 31275—
생성물DalosirvatHCID 5683736112%

반응 조건

온도95 °C

반응 단계

Triethylamine (3.61 mmol) and benzaldehyde (4.3 mmol) in dry dioxane (10 mL) was added to a solution of 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(dimethylamino)propan-1-one (XVI) (5.4 mmol) and 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (0.43 mmol) in dioxane heated at 95° C. under nitrogen. The solution was further heated overnight at 95° C. The solution was cooled and excess solvent was evaporated under vacuum. The residue was partitioned between CH2Cl2 and water. The organic phase was dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography eluting with ethyl acetate in hexane gradient to yield 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-4-phenylbutane-1,4-dione 1 as a white solid (12% yield). 1H NMR (DMSO-d6, 400 MHz): δ ppm 3.33-3.37 (m, 4H), 4.29 (m, 2H), 4.34 (m, 2H), 6.98 (m, 1H), 7.48 (m, 1H), 7.55 (m, 3H), 7.64 (m, 1H), 8.00-8.02 (m, 2H); ESIMS found C18H16O4 m/z 297 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09303010B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-4a814f52ad9f4935a1248735ec214dc4
출처 메모uspto-grants-2016_04