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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 1073865
ノート
印刷プレビュー

反応式

HRID 1073865 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8150Diglyme溶媒

反応条件

温度
150 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-d131f60a008845f6bb8097f6ce4eefa9
出典データセット
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04971982

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート