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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273199생성일: 2026년 10월 25일

Triethylamine → 3-(3',4',5'-Trimethoxybenzoyl)-7-methoxy-8-hydroxy-2h-chromene

https://huagongshe.com/reaction/273199

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-(Dimethylamino)-1-(3,4,5-trimethoxyphenyl)propan-1-oneHCID 412306—
반응물2,3-Dihydroxy-4-methoxybenzaldehydeHCID 11557352—
촉매3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
생성물3-(3',4',5'-Trimethoxybenzoyl)-7-methoxy-8-hydroxy-2h-chromeneHCID 1151626011%

반응 조건

온도115 °C

반응 단계

A mixture of 2-(N,N-dimethylamino)ethyl-(3′,4′,5′-trimethoxyphenyl)ketone (4, 1.17 g, 4.37 mmol), 2,3-dihydroxy-4-methoxybenzaldehyde (2, 0.74 g, 4.37 mmol), 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (0.12 g, 0.44 mmol) and Et3N (1 ml) was heated under reflux at 115° C. for 3.5 hours. After quenching with 1M HCl, the product was extracted with CH2Cl2. The combined extract was washed with water, rinsed with brine and dried over anhydrous magnesium sulfate. Purification was done by silica gel flash column chromatography (60:40, hexane-ethyl acetate) which afforded the pure yellow-colored phenol (0.179 g, 0.48 mmol) in 11% yield. The phenol had a melting point of 189-190° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456214B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-d5ce02cecbb44429899fff1cda686101
출처 메모uspto-grants-2008_11