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Tetrahydrofuran → 5-Chloro-3-methyl-1H-indole-2-carboxylic acid

HRID 379009
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반응식

HRID 379009 반응식
[OH-].[Na+].C([O:5][C:6]([C:8]1[NH:9][C:10]2[C:15]([C:16]=1[CH3:17])=[CH:14][C:13]([Cl:18])=[CH:12][CH:11]=2)=[O:7])C.O1CCCC1>CO>[Cl:18][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:8]([C:6]([OH:7])=[O:5])=[C:16]2[CH3:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 9498591H-Indole-2-carboxylic acid, 5-chloro-3-methyl-, ethyl ester

생성물 1

HCID 31597065-Chloro-3-methyl-1H-indole-2-carboxylic acid

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
25 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

2N NaOH (20 mL) was added to a suspension of 5-chloro-3-methyl-1H-indole-2-carboxylic acid ethyl ester (7.0 g, 29.4 mmol) in methanol (50 mL) and the resulting mixture stirred at 25° C. for 18 hours. Tetrahydrofuran (100 mL) was added and the resulting solution heated at reflux for 30 minutes and concentrated. The residue was dissolved in water and the resulting solution extracted twice with ethyl acetate. The aqueous layer was acidified and the precipitate collected by filtration and washed with water (5.24 g).

후처리

  1. temperaturethe resulting solution heated
  2. temperatureat reflux for 30 minutes
  3. concentrationconcentrated
  4. dissolutionThe residue was dissolved in water
  5. extractionthe resulting solution extracted twice with ethyl acetate
  6. filtrationthe precipitate collected by filtration
  7. washwashed with water (5.24 g)

출처 및 근거

ORD 기록
ord-3c7f72fa70bf480582119993d84dd1f0
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06297269B1

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