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HRID 2212558Erstellt: 25. Oktober 2026

Diethyl dimethylmalonate → 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester

https://huagongshe.com/reaction/2212558

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl dimethylmalonateHCID 15382—
Edukt1-Bromo-4-phenylmethoxybenzeneHCID 138835—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl esterHCID 6959650850,4%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

sec-Butyl lithium (5.85 mL, 7.6 mmol) was added to a solution of 1-bromo-4-benzyloxy-benzene (2.0 g, 7.6 mmol) in THF (10 mL) cooled to −78° C. under nitrogen. The reaction was stirred for 1 h and diethyl dimethylmalonate (4.29 g, 22.8 mmol) was added rapidly. This was stirred for an additional 0.5 h and then allowed to warm to room temperature. The reaction was partitioned between ethyl acetate and 1 N HCl. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give an oil. The product was purified by flash column chromatography (FCC) on silica gel eluting hexane:ethyl acetate (90: 10, v:v) to give 3-(4-benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester (1.25 g, 50%) as an oil. MS found: (M+H)+=327.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07102008B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-5359d81de4724a08af69adbf01961d95
Quellennotizuspto-grants-2006_09