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Ethanol → ethyl 5-phenylpentanoate

HRID 355015
ノート
印刷プレビュー

反応式

HRID 355015 の反応式
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)O.[CH2:19](O)[CH3:20]>>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH2:19][CH3:20])=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH: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

4

反応物 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 16757Benzenepentanoic acid

生成物 1

HCID 234289ethyl 5-phenylpentanoate収率 97.5%

実験手順

250 g (1.4 mols) of 5-phenylvaleric acid are dissolved in 450 ml of absolute ethanol. 114 ml of concentrated sulphuric acid are added to the clear colourless solution and the reaction mixture is refluxed for 48 hours. The reaction mixture, which initially is two-phase, becomes almost homogeneous and separates into two phases again on cooling. The cold two-phase reaction mixture is poured onto diethyl ether and about 1 kg of ice. The aqueous phase is extracted with ether twice more. The ether phases are washed twice with 2 N sodium carbonate solution and twice with NaCl solution. The combined ether phases are dried over MgSO4 and the solvent is removed on a rotary evaporator. After drying under a high vacuum at room temperature, 281.7 g of a colourless oil (97.5% of theory) are obtained.

後処理

  1. temperaturethe reaction mixture is refluxed for 48 hours
  2. temperatureon cooling
  3. customThe cold two-phase reaction mixture
  4. extractionThe aqueous phase is extracted with ether twice more
  5. washThe ether phases are washed twice with 2 N sodium carbonate solution and twice with NaCl solution
  6. dry with materialThe combined ether phases are dried over MgSO4
  7. customthe solvent is removed on a rotary evaporator
  8. customAfter drying under a high vacuum at room temperature

出典と根拠

ORDレコード
ord-48e86c36bba44ae6a123d607a09a520c
出典データセット
uspto-grants-1983_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04377669

反応ノート

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