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

HRID 346807
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HRID 346807 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

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

생성물 1

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

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 962Water용매

실험 절차

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.).

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후처리

  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

출처 및 근거

ORD 기록
ord-ec0baa94779c4a43a1377b4ed448385f
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07173045B2

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