Hydrochloric Acid → HCID 13050370, Verbindung
Reaktionsgleichung
[NH2:1][CH:2]([CH:8]([F:10])[F:9])[CH2:3][CH2:4][C:5]([OH:7])=[O:6].[C:11](Cl)(=[O:13])[CH3:12].Cl>[OH-].[Na+].O1CCOCC1>[F:9][CH:8]([F:10])[CH:2]([NH:1][C:11](=[O:13])[CH3:12])[CH2:3][CH2:4][C:5]([OH:7])=[O:6]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 2 mmole of 4-amino-4-difluoromethylbutyric acid in 5 ml of 1 N sodium hydroxide at 0° C. are added simultaneously from two syringes 160 mg of acetyl chloride diluted in 1 ml of dioxane and 2 ml of 1 N sodium hydroxide. After 30 minutes at 0° C. the solution is acidified by the addition of 6 N hydrochloric acid, then extracted well with dichloromethane. The organic phase is dried and concentrated to afford 4-difluoromethyl-4-(1-oxoethylamino)butyric acid.
Aufarbeitung
- extractionextracted well with dichloromethane
- customThe organic phase is dried
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-fa71501c84834a4db541dea5edd114ac
- Quelldatensatz
- uspto-grants-1982_04
- Patentnummer
- US04326071
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