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Ethylenediamine → HCID 21463158、化合物

HRID 1940979
ノート
印刷プレビュー

反応式

HRID 1940979 の反応式
O=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[C:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:4]([C:18]([OH:20])=O)[O:3]1.[CH2:21]([NH2:24])[CH2:22][NH2:23]>>[O:20]=[C:18]1[C:4]2[N:24]([C:2](=[O:3])[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=3[C:5]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:21][CH2:22][NH:23]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 3301EthylenediamineHCID 42017421-oxo-4-phenyl-1H-isochromene-3-carboxylic acid

生成物 1

HCID 21463158HCID 21463158、化合物

実験手順

A mixture of 1-oxo-4-phenyl-1H-2-benzopyran-3-carboxylic acid (500 mg) and ethylenediamine (15 ml) was stirred at room temperature overnight. After evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml) were added to the residue. The mixture was heated under reflux for 48 hours. To the mixture was added water, and extracted with ethyl acetate. The extract was washed successively with water, aqueous sodium hydrogen carbonate and water, dried, and evaporated to yield the title compound as colorless crystals (115 mg).

後処理

  1. customAfter evaporation of the solvent, concentrated hydrochloric acid (10 ml) and acetic acid (10 ml)
  2. additionwere added to the residue
  3. temperatureThe mixture was heated
  4. temperature
under reflux for 48 hours
  • additionTo the mixture was added water
  • extractionextracted with ethyl acetate
  • washThe extract was washed successively with water, aqueous sodium hydrogen carbonate and water
  • customdried
  • customevaporated
  • 出典と根拠

    ORDレコード
    ord-ea8907fe1ee34b42b5b4d859cd674457
    出典データセット
    uspto-grants-1997_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05700810

    反応ノート

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