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Methanol → 2-Methyl-1-(1-phenylethyl)-1H-indole-3-carboxylic acid

HRID 1526951
ノート
印刷プレビュー

反応式

HRID 1526951 の反応式
CO.[CH3:3][C:4]1[N:5]([CH:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH3:19])[C:6]2[C:11]([C:12]=1[C:13]([O:15]CC)=[O:14])=[CH:10][CH:9]=[CH:8][CH:7]=2.[OH-].[K+]>O>[CH3:3][C:4]1[N:5]([CH:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH3:19])[C:6]2[C:11]([C:12]=1[C:13]([OH:15])=[O:14])=[CH:10][CH:9]=[CH:8][CH:7]=2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 89740220ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate

生成物 1

HCID 897404232-Methyl-1-(1-phenylethyl)-1H-indole-3-carboxylic acid収率 54.8%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a mixed solution of methanol and water (4 mL), ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate (300 mg, 0.98 mmol) and potassium hydroxide (546 mg, 9.76 mmol) was added. The mixture was refluxed with stirring for 4 hours. The reaction mixture was concentrated to give a residue. To the residue, water (10 mL) was added and the mixture was extracted with dichloromethane (20 mL×3). The organic phase was concentrated to give crude product 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylic acid (150 mg). LRMS (M−H)− m/z: calcd 279.13. found 279.

後処理

  1. temperatureThe mixture was refluxed
  2. concentrationThe reaction mixture was concentrated
  3. customto give a residue
  4. extractionthe mixture was extracted with dichloromethane (20 mL×3)
  5. concentrationThe organic phase was concentrated

出典と根拠

ORDレコード
ord-a9d918f1177f42d5b65d2cad50cc21c7
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085583B2

反応ノート

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