Potassium Permanganate → HCID 59425724, 화합물

HRID 502130노트

반응식

HRID 502130 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:13]=[C:12]2[C:8]([C:9]([CH:16]=[O:17])=[CH:10][N:11]2[CH2:14][CH3:15])=[CH:7][CH:6]=1)=[O:4].[O-:18][Mn](=O)(=O)=O.[K+]>CC(C)=O.O>[CH3:1][O:2][C:3]([C:5]1[CH:13]=[C:12]2[C:8]([C:9]([C:16]([OH:18])=[O:17])=[CH:10][N:11]2[CH2:14][CH3:15])=[CH:7][CH:6]=1)=[O:4]

참가 물질

5

반응물 2

HCID 516875Potassium Permanganate2회HCID 59425156Methyl 1-ethyl-3-formyl-1H-indole-6-carboxylate

생성물 1

HCID 59425724HCID 59425724, 화합물수율 80.4%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매2회

실험 절차

1-Ethyl-3-formyl-1H-indole-6-carboxylic acid methyl ester (800 mg, 3.5 mmol), prepared as shown in example 1P, step A, is dissolved in acetone (98 mL). A solution of KMnO4(655 mg, 4.15 mmol) in H2O (31 mL) is added. The reaction mixture is stirred at room temperature for 90 minutes. Another addition of KMnO4 (108 mg) in H2O (6 mL), followed by stirring for another 45 minutes is required to drive the reaction to completion. The reaction mixture is then quenched with 10% H2O2 (1.5 mL). The mixture is filtered through celite. The filtrate is stripped down under vacuum to roughly ⅓ of the volume. The residue is acidified with 6N HCl, and is extracted into ethyl acetate. The solids isolated from the ethyl acetate layer are triturated with acetone to yield 1-ethyl-1H-indole-3,6-dicarboxylic acid 6-methyl ester (696 mg, 79%) as a light orange solid.

후처리

  1. stirringby stirring for another 45 minutes
  2. customthe reaction to completion
  3. customThe reaction mixture is then quenched with 10% H2O2 (1.5 mL)
  4. filtrationThe mixture is filtered through celite
  5. extractionis extracted into ethyl acetate
  6. customThe solids isolated from the ethyl acetate layer
  7. customare triturated with acetone

출처 및 근거

ORD 기록
ord-c829c93d7bc14ee881bf433328eb6db0
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07772271B2

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