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Sodium Hydroxide → 6-Chloro-1,2,3,4-tetrahydrocarbazole-2-carboxylic acid

HRID 436506
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반응식

HRID 436506 반응식
C([N:9]1[C:21]2[CH2:20][CH:19]([C:22]([OH:24])=[O:23])[CH2:18][CH2:17][C:16]=2[C:15]2[C:10]1=[CH:11][CH:12]=[C:13]([Cl:25])[CH:14]=2)(=O)C1C=CC=CC=1.[OH-].[Na+]>>[Cl:25][C:13]1[CH:14]=[C:15]2[C:10](=[CH:11][CH:12]=1)[NH:9][C:21]1[CH2:20][CH:19]([C:22]([OH:24])=[O:23])[CH2:18][CH2:17][C:16]2=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14798Sodium HydroxideHCID 21452699HCID 21452699, 화합물

생성물 1

HCID 214527126-Chloro-1,2,3,4-tetrahydrocarbazole-2-carboxylic acid

실험 절차

A stirred mixture of 100 mg. of 9-benzoyl-6-chloro-1,2,3,4-tetrahydrocarbazole-2-carboxylic acid and 5 ml. of 3N sodium hydroxide was heated on a steam bath for 5 minutes and cooled to room temperature. After 1 hour at room temperature, the reaction mixture was further cooled in an ice bath, filtered and the filter cake was washed with 10 drops of cold water. The filter cake was dissolved in 20 ml. of warm water, and the resulting warm solution was made strongly acid with 1N hydrochloric acid. Following filtration, washing with warm water and drying, 56 mg. of (±) 6-chloro-1,2,3,4-tetrahydrocarbazole-2-carboxylic acid was obtained, m.p. 247°-249°.

후처리

  1. additionA stirred mixture of 100 mg
  2. temperaturethe reaction mixture was further cooled in an ice bath
  • filtrationfiltered
  • washthe filter cake was washed with 10 drops of cold water
  • dissolutionThe filter cake was dissolved in 20 ml
  • temperatureof warm water, and the resulting warm solution
  • filtrationfiltration
  • washwashing with warm water
  • customdrying
  • 출처 및 근거

    ORD 기록
    ord-40126086251746908ff1779916af4c97
    출처 데이터셋
    uspto-grants-1977_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04009181

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