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HCID 53637082, 화합물 → 1-(2,4-Dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)-2-propen-1-one

HRID 2254256
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HRID 2254256 반응식
COC[O:4][C:5]1[CH:28]=[C:27]([O:29]COC)[CH:26]=[CH:25][C:6]=1[C:7](=[O:24])[CH:8]=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([O:16]COC)=[C:12]([O:20]COC)[CH:11]=1>Cl.CO>[OH:4][C:5]1[CH:28]=[C:27]([OH:29])[CH:26]=[CH:25][C:6]=1[C:7](=[O:24])[CH:8]=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[C:12]([OH:20])[CH:11]=1
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참가 물질

3

반응물 1

HCID 53637082HCID 53637082, 화합물

생성물 1

HCID 24831-(2,4-Dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)-2-propen-1-one수율 22.4%

시약·촉매·용매 1

HCID 21893726Hydrochloride methanol용매

실험 절차

Then, 4.0 g of the so-obtained 2',3,4,4'-tetrakis(methoxymethoxy)chalcone was dissolved in 36 ml of a hydrochloric acid/methanol reagent, and the solution was refluxed for 10 minutes. The reaction liquid was poured into ice water, and the precipitated crystal was recovered by filtration, washed with water, dried and subjected to the column chromatograpy 280 g of 230-400 mesh Kieselgel, eluting solvent=hexane/ethyl acetate (1/1), 0.4 kg/cm2). Fractions of 50 ml were collected, and the 32th to 70th fractions were combined to obtain 543.2 mg (yield=22.1%) of 2',3,4,4'-tetrahydroxychalcone.

후처리

  1. temperaturethe solution was refluxed for 10 minutes
  2. customThe reaction liquid
  3. filtrationthe precipitated crystal was recovered by filtration
  4. washwashed with water
  5. customdried
  6. washeluting solvent=hexane/ethyl acetate (1/1), 0.4 kg/cm2)
  7. customFractions of 50 ml were collected

출처 및 근거

ORD 기록
ord-6144360c524f4405b9075c5762e527d3
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05234951

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