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Sodium Hydroxide → 4-Ethoxybutanoic acid

HRID 591122
ノート
印刷プレビュー

反応式

HRID 591122 の反応式
[CH2:1]([O:3][CH2:4][CH2:5][CH2:6][C:7]([O:9]CC)=[O:8])[CH3:2].[OH-].[Na+]>O1CCCC1>[CH2:1]([O:3][CH2:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8])[CH3:2]
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 2

HCID 14798Sodium HydroxideHCID 4424983Ethyl 4-ethoxybutyrate

生成物 1

HCID 211920454-Ethoxybutanoic acid収率 72.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To an ice cold stirred solution of ethyl 4-ethoxybutanoate (30) (˜1 g) in 10 mL of tetrahydrofuran (THF) was added aqueous NaOH solution (0.62 g in 7 ml of H2O) and stirred at room temperature for 12 h, while monitoring the reaction by TLC. Most of the solvent was evaporated under reduced pressure and the residue was diluted with water (10 mL). The aqueous layer was acidified with 1N HCl solution (PH˜2) and then extracted with ethyl acetate (15 mL×3). The combined organic extracts was dried over anhydrous Na2SO4 and concentrated under vacuum to yield 0.6 g (73.14) of 4-ethoxybutanoic acid as light yellow oil. 1HNMR (400 MHz, CDCl3): δ 1.20 (t, J=9.2 Hz, 3H); 1.87-1.95 (m, 2H); 2.47 (t, J=10 Hz; 2H); 3.48 (q, J=9.2 Hz, 4H).

後処理

  1. customthe reaction by TLC
  2. customMost of the solvent was evaporated under reduced pressure
  3. additionthe residue was diluted with water (10 mL)
  4. extractionextracted with ethyl acetate (15 mL×3)
  5. dry with materialThe combined organic extracts was dried over anhydrous Na2SO4
  6. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-3a5326518f024e21aa9627d4d622f96f
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09238625B2

反応ノート

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