Water → ethyl 4-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)butanoate

HRID 83991ノート

反応式

HRID 83991 の反応式
[N:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[C:4](=[O:11])[NH:3][N:2]=1.Br[CH2:13][CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17].C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[O:11]=[C:4]1[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=2[N:1]=[N:2][N:3]1[CH2:13][CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17]

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 76300Ethyl 4-bromobutyrateHCID 1354087931,2,3-Benzotriazin-4(1H)-one

生成物 1

HCID 60262901ethyl 4-(4-oxo-1,2,3-benzotriazin-3(4H)-yl)butanoate収率 76.6%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

In a dry round bottom flask, 1,2,3-benzotriazin-4(3H)-one (50 g), ethyl 4-bromobutanoate (86.2 g) and potassium carbonate (141 g) were taken and dissolved in dimethylformamide (350 mL) and heated to 60° C. to 70° C. for 3 to 4 hours. After cooling to room temperature, water was added to the reaction mixture and extracted with ethyl acetate. The combined organic layer was washed with water and brine and dried over anhydrous sodium sulfate. Solvents were evaporated under reduced pressure and the crude product was purified by silica gel flash column chromatography over silica gel using 20% ethylacetate in hexane as eluant to afford the title compound (68 g).

後処理

  1. temperatureheated to 60° C. to 70° C. for 3 to 4 hours
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layer was washed with water and brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customSolvents were evaporated under reduced pressure
  6. customthe crude product was purified by silica gel flash column chromatography over silica gel using 20% ethylacetate in hexane as eluant

出典と根拠

ORDレコード
ord-13bd807ba44c49f9aefa47a749fd56a1
出典データセット
uspto-grants-2014_09
特許番号
US08846910B2

反応ノート

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