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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2164434Erstellt: 26. Oktober 2026

Diethyl Ether → 3-(1,3-Dioxolan-2-YL)benzophenone

https://huagongshe.com/reaction/2164434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt2-BenzoylbenzaldehydeHCID 161195—
EduktSodium BicarbonateHCID 516892—
EduktHCID 13195968HCID 13195968—
KatalysatorPyridineHCID 1049—
Katalysator(Trimethylsilyl)methyl Trifluoromethanesulfonate [Trimethylsilylmethylating Reagent]HCID 2760857—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(1,3-Dioxolan-2-YL)benzophenoneHCID 10515088—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a stirred solution of benzoylbenzaldehyde (2 g, 10 mmol) and 1,2-bis-(trimethoxysiloxy)ethane (2.3 g, 11 mmol) in dry dichloromethane (30 cm3) under N2 at room temperature was added trimethylsilylmethyl trifluoromethanesulphonate (5 drops). After stirring at 20° C. for 48 hours, pyridine (3 drops) was added followed by saturated NaHCO3 (20 cm3) and diethyl ether (20 cm3). The resulting mixture was stirred for 30 minutes. The ethereal layer was separated off and the aqueous layer extracted twice more with diethyl ether. The combined extracts were washed with water, dried over a mixture of anhydrous Na2CO3 and anhydrous Na2SO4 (1:1) and the solvent removed in vacuo to give 2-(3-benzoylphenyl)-1,3-dioxolane, nD20 1.5890. Yield 2.2 g (91.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04504491
Quelldatensatzuspto-grants-1985_03
ORD IDord-2ae659d81b1c46e0943d7a38d3145739
Quellennotizuspto-grants-1985_03