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Potassium Hydroxide → (5-fluoro-2-methyl-1H-indol-3-yl)acetic acid

HRID 346807
ノート
印刷プレビュー

反応式

HRID 346807 の反応式
C([O:3][C:4](=[O:17])[CH2:5][C:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([F:15])[CH:13]=2)[NH:8][C:7]=1[CH3:16])C.[OH-].[K+]>CO.O>[F:15][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([CH3:16])=[C:6]2[CH2:5][C:4]([OH:17])=[O:3]
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 2

HCID 14797Potassium HydroxideHCID 11665843Ethyl (5-fluoro-2-methyl-1H-indol-3-yl)acetate

生成物 1

HCID 2772338(5-fluoro-2-methyl-1H-indol-3-yl)acetic acid

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回HCID 962Water溶媒

実験手順

This ester (4.5 g, 0.019 mol.) was added to a solution of KOH (2.13 g, 38 mmol.) in methanol (100 ml), and the mixture was heated at reflux for 30 min. For working up, the mixture was diluted with water (100 ml) and methanol was distilled off using a rotary evaporator. The aqueous phase was adjusted to pH 4 with 2M HCl and stored for 2 h at 4° C. The white solid that precipitated was filtered off with suction and washed with methanol. (5-Fluoro-2-methyl-1H-indol-3-yl)acetic acid was obtained in a yield of 3.25 g (m.p. 136–138° C.).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 30 min
  3. distillationwas distilled off
  4. customa rotary evaporator
  5. customThe white solid that precipitated
  6. filtrationwas filtered off with suction
  7. washwashed with methanol

出典と根拠

ORDレコード
ord-ec0baa94779c4a43a1377b4ed448385f
出典データセット
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07173045B2

反応ノート

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