Water → 2-Benzyloxycarbonylmethyl-2-(pyrrol-1-yl)malonic acid diethyl ester

HRID 256582

Reaktionsgleichung

[CH2:1]([O:3][C:4](=[O:16])[CH:5]([N:11]1[CH:15]=[CH:14][CH:13]=[CH:12]1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH3:2].[H-].[Na+].Br[CH2:20][C:21]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22].O>CN(C)C=O>[CH2:9]([O:8][C:6](=[O:7])[C:5]([CH2:20][C:21]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22])([N:11]1[CH:12]=[CH:13][CH:14]=[CH:15]1)[C:4]([O:3][CH2:1][CH3:2])=[O:16])[CH3:10]

Komponenten

Reaktionsbedingungen

Temperatur: 25 °C

Versuchsvorschrift

To a stirred solution of 2-(pyrrol-1-yl)malonic acid diethyl ester (53.0 g) in anhydrous dimethylformamide (300 ml) was added portionwise sodium hydride (63% dispersion in mineral oil, 10.0 g) under ice cooling. The resulting mixture was stirred at 25° C. for 30 minutes and thereto was added benzyl bromoacetate (70.1 g). After stirring at 25° C. for 15 hours, the reaction mixture was poured into water and extracted with ethyl acetate. The extracts were dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was chromatographed on silica gel using n-hexane/ethyl acetate (10:1) as the eluent. Fractions containing the title compound were pooled and evaporated under reduced pressure to give the title compound (80.0 g, 91.0%) as a colorless oil.

Aufarbeitung

stirringAfter stirring at 25° C. for 15 hours
extractionextracted with ethyl acetate
dry with materialThe extracts were dried over anhydrous sodium sulfate
concentrationconcentrated under reduced pressure
customThe residue was chromatographed on silica gel
additionFractions containing the title compound
customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag: ord-38ce61e43bf8439dbd7adef44aa9a625
Quelldatensatz: uspto-grants-1993_11
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05258382

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