2-Ketobutyric acid methyl ester → Methyl 2-(2-fluoro-3-methyl-4-pyridinyl)-2-hydroxybutanoate

HRID 47355

Reaktionsgleichung

C([Li])CCC.[F:6][C:7]1[C:12]([CH3:13])=[C:11](I)[CH:10]=[CH:9][N:8]=1.[O:15]=[C:16]([CH2:21][CH3:22])[C:17]([O:19][CH3:20])=[O:18].O.C1COCC1>CCCCCC.C1COCC1>[F:6][C:7]1[C:12]([CH3:13])=[C:11]([C:16]([OH:15])([CH2:21][CH3:22])[C:17]([O:19][CH3:20])=[O:18])[CH:10]=[CH:9][N:8]=1

Komponenten

Reaktionsbedingungen

Temperatur: -78 °C

Versuchsvorschrift

6.9 ml (11 mmol) of 1.6M butyllithium in hexane are added dropwise to a solution, stirred at −78° C. of 2.6 g (11 mmol) of 2-fluoro-4-iodo-3-methylpyridine (described in J.O.C., 1993, 58, pp. 7832) in 100 ml of THF. The reaction mixture is then stirred for 10 minutes at −78° C. before the addition of a solution of 1.5 g (12.9 mmol) of methyl 2-oxo-butyrate in 20 ml of THF. The reaction mixture is stirred for 10 minutes at −78° C., and then hydrolysed with a mixture of water/THF. The aqueous phase is decanted and then extracted 3 times with 50 ml of methyl acetate each time. The combined organic phases are dried, concentrated and purified by chromatography over silica (eluant dichloromethane/acetone 95/5) to yield the expected product.

Aufarbeitung

customThe aqueous phase is decanted
extractionextracted 3 times with 50 ml of methyl acetate each time
customThe combined organic phases are dried
concentrationconcentrated
custompurified by chromatography over silica (eluant dichloromethane/acetone 95/5)

Quellen und Nachweise

ORD-Eintrag: ord-c3e61e1cf6d644b09d152747e13243a8
Quelldatensatz: uspto-grants-2004_03
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US06699876B2

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