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Ethanol → 3'-Cyano flavanone

HRID 1733290
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HRID 1733290 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=[O:7])#[N:2].O[CH2:12][C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:14].C(O)C>O>[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]1[CH2:12][C:13](=[O:14])[C:15]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[O:7]1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 68490alpha-HydroxyacetophenoneHCID 90670m-Formylbenzonitrile

생성물 1

HCID 545536863'-Cyano flavanone수율 10.6%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 3-cyanobenzaldehyde (25 g, 0.19 mol), 2-hydroxyacetophenone (25.9 g. 0.19 mol), 38.1 g (0.1 mol) of borax, 250 ml of ethanol, and 250 ml of H2O was refluxed for four days. When cool the reaction mixture was diluted with H2O and extracted with ethyl acetate. The ethyl acetate was dried over anhydrous Na2SO4, filtered, and evaporated to give a dark, tarry residue. The residue was chromatographed on 1 kg of silica gel, eluting with benzene. From this was isolated 5 g of 3'-cyano flavanone as an oil.

후처리

  1. temperaturewas refluxed for four days
  2. temperatureWhen cool the reaction mixture
  3. extractionextracted with ethyl acetate
  4. dry with materialThe ethyl acetate was dried over anhydrous Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customto give a dark, tarry residue
  8. customThe residue was chromatographed on 1 kg of silica gel
  9. washeluting with benzene

출처 및 근거

ORD 기록
ord-f7bded1ec96347c5b60a216e95b4a2a1
출처 데이터셋
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04241069

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