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1-(2-Hydroxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol → 2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran

HRID 892503
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인쇄 미리보기

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HRID 892503 반응식
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1)(O)[CH:9]=[C:10]([CH3:12])[CH3:11]>COCCOCCOC>[CH3:11][C:10]1([CH3:12])[CH:9]=[C:8]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[O:1]1
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참가 물질

3

반응물 1

HCID 198956121-(2-Hydroxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol

생성물 1

HCID 187551522,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran수율 58.4%

시약·촉매·용매 1

HCID 8150Diglyme용매

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온도
150 °C

실험 절차

4.42 g of 1-(2-hydroxyphenyl)-3-methyl-1-(2-pyridyl)-2-buten-1-ol were dissolved in 70 ml of diethylene glycol dimethyl ether and heated at 150° C. for 2 hours. The mixture was allowed to cool to room temperature, the solvent was removed by evaporation and the residue was partitioned between ethyl acetate and sodium chloride solution. The organic phase was dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:4) for the elution to give 2.4 g of 2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran of melting point 80°-82° C.

후처리

  1. temperatureto cool to room temperature
  2. customthe solvent was removed by evaporation
  3. customthe residue was partitioned between ethyl acetate and sodium chloride solution
  4. dry with materialThe organic phase was dried over sodium sulphate
  5. customevaporated
  6. customThe residue was chromatographed on silica gel
  7. washfor the elution

출처 및 근거

ORD 기록
ord-6d07d9c9588247f099ec5dd0127aaac0
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05118694

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