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

HRID 436506
ノート
印刷プレビュー

反応式

HRID 436506 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 14798Sodium HydroxideHCID 21452699HCID 21452699、化合物

生成物 1

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

実験手順

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°.

後処理

  1. additionA stirred mixture of 100 mg
  2. temperaturethe reaction mixture was further cooled in an ice bath
filtration
filtered
  • 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
  • 出典と根拠

    ORDレコード
    ord-40126086251746908ff1779916af4c97
    出典データセット
    uspto-grants-1977_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04009181

    反応ノート

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