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Sodium Hydroxide → 4-Ethoxybutanoic acid

HRID 591122
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HRID 591122 반응식
[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]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 4424983Ethyl 4-ethoxybutyrate

생성물 1

HCID 211920454-Ethoxybutanoic acid수율 72.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-3a5326518f024e21aa9627d4d622f96f
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238625B2

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