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Sodium Hydroxide → 3-chloro-4-(N-(3-indolylcarbonyl)amino)phenylacetic acid

HRID 1372600
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HRID 1372600 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:20][C:21]([O:23]CC)=[O:22])[CH:5]=[CH:6][C:7]=1[NH:8][C:9]([C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1)=[O:10].[OH-].[Na+]>C1COCC1.Cl>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:20][C:21]([OH:23])=[O:22])[CH:5]=[CH:6][C:7]=1[NH:8][C:9]([C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 17858762Ethyl 3-chloro-4-(3-indolylcarbonylamino)phenylacetate

생성물 1

HCID 178594403-chloro-4-(N-(3-indolylcarbonyl)amino)phenylacetic acid수율 91.3%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of ethyl 3-chloro-4-(3-indolylcarbonylamino)phenylacetate (1.25 g, 3.50 mmol) in THF (35 mL) was added 0.25N NaOH (21 mL, 5.23 mmol) under stirring. The reaction mixture was then stirred at room temperature for 24 hours. The reaction mixture was poured in 1N HCl (30 ml) under stirring at 0° C. The crystals thus precipitated were collected by filtration, whereby 3-chloro-4-(N-(3-indolylcarbonyl)amino)phenylacetic acid (1.05 g, 91%) was obtained as a colorless solid.

후처리

  1. stirringThe reaction mixture was then stirred at room temperature for 24 hours
  2. stirringunder stirring at 0° C
  3. customThe crystals thus precipitated
  4. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-14359ea9a84e4d1d86fbeea32e6294f6
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157487B2

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