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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33956생성일: 2026년 10월 24일

Ethyl Acetate → (2,3-Dihydroxy-4-methoxy-phenyl)-(1,2,3-trimethoxy-8,9-dihydro-7H-benzocyclohepten-5-yl)-methanone

https://huagongshe.com/ko/reaction/33956

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물1,4-CyclohexadieneHCID 12343—
반응물(2,3-Bis-benzyloxy-4-methoxy-phenyl)-(1,2,3-trimethoxy-8,9-dihydro-7H-benzocyclohepten-5-yl)-methanoneHCID 68920825—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물(2,3-Dihydroxy-4-methoxy-phenyl)-(1,2,3-trimethoxy-8,9-dihydro-7H-benzocyclohepten-5-yl)-methanoneHCID 1598632363%

반응 조건

온도25 °C

반응 단계

95 (0.69 g, 1.19 mmol) was dissolved in 20 mL of anhydrous EtOH under nitrogen and the reaction mixture was immersed in a water bath to maintain a temperature of 25° C. 1.2 g of Pd—C was added followed by 1,4-cyclohexadiene (1.13 mL, 11.90 mmol) and the reaction mixture was stirred for 7 h. The reaction mixture was monitored for completion by TLC (Rf: 0.32, 60:40 Hex:EA). The reaction mixture was filtered through celite, washed with ethylacetate, rotavaped and purified by column chromatography (20:80 EtOAc:Hexanes) to obtain 0.3 g (63%) of 23 as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429681B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1618bf0e6699400c86ae13927af39f95
출처 메모uspto-grants-2008_09