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Ethanol → ethyl 2,3-dihydro-1H-indene-2-carboxylate

HRID 868011
ノート
印刷プレビュー

反応式

HRID 868011 の反応式
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1([C:13]([OH:15])=[O:14])C(O)=O.S(=O)(=O)(O)O.[CH2:21](O)[CH3:22]>>[CH2:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1][CH:2]1[C:13]([O:15][CH2:21][CH3:22])=[O:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 2519571,3-Dihydroindene-2,2-dicarboxylic acid

生成物 1

HCID 15280733ethyl 2,3-dihydro-1H-indene-2-carboxylate

実験手順

11.7 g of 2,2-indandicarboxylic acid was heated at 200° C. for 30 minutes. After liberation of bubbles ceased, the reaction product was cooled and dissolved in 150 ml of ethanol. 4 ml of concentrated sulfuric acid was added to the solution and the mixture was heated under reflux for 4 hours. The reaction mixture was concentrated in vacuo and the residue was neutralized by addition of sodium carbonate. The mixture was extracted with chloroform. The extract was washed with water and dried and then concentrated in vacuo to give 9.4 g of ethyl 2-indancarboxylate as an oil.

後処理

  1. temperature
このページの内容参加物実験手順後処理出典と根拠反応ノート
the reaction product was cooled
  • temperaturethe mixture was heated
  • temperatureunder reflux for 4 hours
  • concentrationThe reaction mixture was concentrated in vacuo
  • additionthe residue was neutralized by addition of sodium carbonate
  • extractionThe mixture was extracted with chloroform
  • washThe extract was washed with water
  • customdried
  • concentrationconcentrated in vacuo
  • 出典と根拠

    ORDレコード
    ord-4ee1dc758ad949999eddc9640d0788c7
    出典データセット
    uspto-grants-1988_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04777257

    反応ノート

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