Ethylene Glycol → 2-(5-Methyl-7-nitro-1-indolinyl)benzoic acid

HRID 4023

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HRID 4023 반응식
[OH-:1].[K+].[CH3:3][C:4]1[CH:5]=[C:6]2[C:10](=[C:11]([N+:13]([O-:15])=[O:14])[CH:12]=1)[N:9]([C:16]1C=[CH:22][CH:21]=[CH:20][C:17]=1C#N)[CH2:8][CH2:7]2.ClCCl.[CH2:27]([OH:30])[CH2:28]O>O>[CH3:3][C:4]1[CH:5]=[C:6]2[C:10](=[C:11]([N+:13]([O-:15])=[O:14])[CH:12]=1)[N:9]([C:16]1[CH:17]=[CH:20][CH:21]=[CH:22][C:28]=1[C:27]([OH:30])=[O:1])[CH2:8][CH2:7]2

참가 물질

6

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온도
175 °C

실험 절차

A stirred solution under nitrogen of potassium hydroxide (30 g, 0.53 mole) in ethylene glycol (250 ml) and water (35 ml) was heated to 175° C., at which temperature there was added 2-(5-methyl-7-nitroindolin-1-yl)benzonitrile (26 g, 0.093 mole). After heating at 175° C. for 3 hours, the reaction mixture was cooled to room temperature and dichloromethane (1 liter) and water (500 ml), were added, with stirring. The aqueous phase was separated and extracted with two 250 ml-portions of dichloromethane. The aqueous phase was then cooled in an ice-bath and acidified with concentrated hydrochloric acid. The product was extracted out with three 500 ml-portions of dichloromethane. The combined organic extracts were washed twice with brine, dried, filtered, and concentrated to afford 9.0 g (32%) of product.

후처리

  1. temperaturethe reaction mixture was cooled to room temperature
  2. customThe aqueous phase was separated
  3. extractionextracted with two 250 ml-portions of dichloromethane
  4. temperatureThe aqueous phase was then cooled in an ice-bath
  5. extractionThe product was extracted out with three 500 ml-portions of dichloromethane
  6. washThe combined organic extracts were washed twice with brine
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c00a9480d9f0457d8175dcbd5a9b8e1d
출처 데이터셋
uspto-grants-1988_02
특허 번호
US04723007

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