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Potassium Hydroxide → 3-(4-Chlorophenyl)-4-(methylsulfanyl)-1h-indole-2-carboxylic acid

HRID 857319
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인쇄 미리보기

반응식

HRID 857319 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[S:17][CH3:18])[NH:10][C:9]=2[C:19]([O:21]CC)=[O:20])=[CH:4][CH:3]=1.[OH-].[K+]>CCO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[S:17][CH3:18])[NH:10][C:9]=2[C:19]([OH:21])=[O:20])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 21867418Ethyl 3-(4-chlorophenyl)-4-(methylsulfanyl)-1h-indole-2-carboxylate

생성물 1

HCID 218674693-(4-Chlorophenyl)-4-(methylsulfanyl)-1h-indole-2-carboxylic acid수율 101.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of the ester of Step 4 (1.5 g) in EtOH (15 mL) was added 1N KOH solution (13 mL). The reaction mixture was stirred at reflux for 1 hour. The organic solvent was removed by evaporation and the aqueous solution was acidified with 3N HCl and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated to give the title compound as a white solid (1.4 g).

후처리

  1. temperatureat reflux for 1 hour
  2. customThe organic solvent was removed by evaporation
  3. extractionextracted with EtOAc
  4. dry with materialThe combined organic layers were dried over Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2488214679e247d4b97f79b0d5521fa6
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07144913B2

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