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Ethanol → Ethyl 1H-indole-3-acetate

HRID 344716
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HRID 344716 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11]([OH:13])=[O:12])=[CH:2]1.S(=O)(=O)(O)O.[OH-].[Na+].[CH2:21](O)[CH3:22]>>[CH2:21]([O:12][C:11]([CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1)=[O:13])[CH3:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 702EthanolHCID 802Indole-3-Acetic AcidHCID 1118Sulfuric AcidHCID 14798Sodium Hydroxide

생성물 1

HCID 13067Ethyl 1H-indole-3-acetate수율 90%

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온도
0 °C

실험 절차

A mixture of 5.0 g (28.5 mmols) of indole-3acetic acid, 250 ml of ethanol and 5 ml of conc. sulfuric acid was heated under reflux for 2 hours. After cooling to 0° C., the mixture was neutralized with a 2 normal aqueous sodium hydroxide solution. The solvent was evaporated under reduced pressure, and then water was added to the residue followed by extraction of the solution with chloroform. The chloroform layer was washed with an aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was dried to afford 5.2 g (yield: 90%) of the title compound.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hours
  3. customThe solvent was evaporated under reduced pressure
  4. additionwater was added to the residue
  5. extractionfollowed by extraction of the solution with chloroform
  6. washThe chloroform layer was washed with an aqueous saturated sodium chloride solution
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was evaporated under reduced pressure
  9. customthe residue was dried

출처 및 근거

ORD 기록
ord-1713a83d80b14f36bfc94b17e470b70f
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05053408

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