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Ethanol → Ethyl 3-(4-methoxybenzoyl)propionate

HRID 1110019
ノート
印刷プレビュー

反応式

HRID 1110019 の反応式
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]([C:7]([CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[O:8])=[CH:5][CH:4]=1.S(=O)(=O)(O)O.[CH2:21](O)[CH3:22]>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]([CH2:9][CH2:10][C:11]([O:13][CH2:21][CH3:22])=[O:12])=[O:8])=[CH:14][CH:15]=1
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 766134-Methoxy-gamma-oxobenzenebutanoic acid

生成物 1

HCID 585132Ethyl 3-(4-methoxybenzoyl)propionate

実験手順

21 g of 3-(4-methoxybenzoyl)propionic acid were heated under reflux for 51/4 hours in 350 ml of ethanol after addition of 7.3 ml of concentrated sulfuric acid The reaction mixture was worked up by concentrating it, taking up the remaining residue in 100 ml of water and extracting the mixture with dichloromethane. The organic phase was separated, washed with 50 ml of saturated aqueous sodium bicarbonate solution, then washed with water until neutral, dried and concentrated. 23.3 g of crude ethyl 3-(4-methoxybenzoyl)-propionate were obtained as a yellowish, crystallizing oil.

後処理

  1. concentration
by concentrating it
  • extractionextracting the mixture with dichloromethane
  • customThe organic phase was separated
  • washwashed with 50 ml of saturated aqueous sodium bicarbonate solution
  • washwashed with water until neutral,
  • customdried
  • concentrationconcentrated
  • 出典と根拠

    ORDレコード
    ord-b53944b32fa44caa99cf3ba0cc6fea17
    出典データセット
    uspto-grants-1994_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05324725

    反応ノート

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