Sodium Hydroxide → 4-(Pyridin-4-yl)butanoyl-sarcosine
Reaktionsgleichung
C([O:3][C:4](=[O:19])[CH2:5][N:6]([C:8](=[O:18])[CH2:9][CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=1)[CH3:7])C.[OH-].[Na+]>CCO>[N:15]1[CH:14]=[CH:13][C:12]([CH2:11][CH2:10][CH2:9][C:8]([N:6]([CH2:5][C:4]([OH:19])=[O:3])[CH3:7])=[O:18])=[CH:17][CH:16]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Ester 6-1 (324 mg, 1.22 mmol) was dissolved in 6 mL EtOH, then 1 N NaOH (2.4 mL, 2.4 mmol) was added. After stirring overnight the mixture was concentrated, rediluted with EtOAc, extracted into 10% KHSO4, then concentrated, providing acid 6-2, along with inorganic salts.
Aufarbeitung
- concentrationwas concentrated
- additionrediluted with EtOAc
- extractionextracted into 10% KHSO4
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-d5a8552b1a9340628cadcb3f5461aec2
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05952306
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