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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 569362Erstellt: 24. Oktober 2026

Acetic acid, 2-chloro-, phenylmethyl ester → Tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate

https://huagongshe.com/de/reaction/569362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic acid, 2-chloro-, phenylmethyl esterHCID 8786—
EduktPotassium CarbonateHCID 11430—
Edukttert-butyl 2-hydroxyimino-3-oxobutanoateHCID 178468384—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrateHCID 5381166595,3%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a suspension of tert-butyl 2-hydroxyimino-3-oxobutyrate (56.4 g) and potassium carbonate (62.4 g) in ethyl acetate (300 ml) and N,N-dimethylformamide (60 ml) was added benzyl chloroacetate (60 g), and the mixture was stirred at 40° C. for 7 hours. The reaction mixture was poured into ice-water (1000 ml), and the separated organic layer was washed twice with a saturated aqueous solution of sodium chloride and then dried over magnesium sulfate. Removal of the solvent gave tert-butyl 2-benzyloxycarbonylmethoxyimino-3-oxobutyrate (96.3 g) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04731443
Quelldatensatzuspto-grants-1988_03
ORD IDord-3228b8bd8b25419a9f5eca11a38f91e4
Quellennotizuspto-grants-1988_03