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Sodium Hydroxide → 4-Ethoxybutanoic acid

HRID 591122
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 591122
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 4424983Ethyl 4-ethoxybutyrate

Produkt 1

HCID 211920454-Ethoxybutanoic acidAusbeute 72,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-3a5326518f024e21aa9627d4d622f96f
Quelldatensatz
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09238625B2

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