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Tetrahydrofuran → (S)-2-(2-Oxo-2H-pyridin-1-yl)-propionic acid

HRID 2065484
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2065484
C([O:3][C:4](=[O:14])[C@@H:5]([N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]1=[O:13])[CH3:6])C.C1COCC1.[OH-].[Na+]>O>[O:13]=[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][N:7]1[C@@H:5]([CH3:6])[C:4]([OH:14])=[O:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 66650045(S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester

Produkt 1

HCID 53628857(S)-2-(2-Oxo-2H-pyridin-1-yl)-propionic acidAusbeute 27 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A stirred mixture of (S)-2-(2-Oxo-2H-pyrid-1-yl)-propionic acid ethyl ester (364 mg, 1.87 mmol), THF (2 ml), water (1 ml) and sodium hydroxide (90 mg, 2.24 mmol) was kept at room temperature for 1 h, then concentrated under reduced pressure. The residue was dissolved in ether and the resulting solution washed with water. The organic layer was discarded and the aqueous layer was acidified with concentrated HCl then extracted several times with ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was triturated with ether to afford the title compound as a colorless solid (84 mg, 27%): [α]31D=−50° (c=0.2, CH3OH); 1H NMR (400 MHz, DMSO) δ 1.5 (3H, d), 5.1 (1H, q), 6.2 (1H, t), 6.4 (1H, d), 7.4 (1H, m), 7.6 (1H, d).

Aufarbeitung

  1. concentrationconcentrated under reduced pressure
  2. dissolutionThe residue was dissolved in ether
  3. washthe resulting solution washed with water
  4. extractionthen extracted several times with ethyl acetate
  5. dry with materialThe combined organic extracts were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was triturated with ether

Quellen und Nachweise

ORD-Eintrag
ord-92433ac00bc14c73b8f8770be62ed2fb
Quelldatensatz
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08288537B2

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