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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1757501Erstellt: 24. Oktober 2026

N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one

https://huagongshe.com/de/reaction/1757501

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methoxy-N-methylbenzamideHCID 569575—
Edukt1-Ethynyl-3-((4-methoxybenzyl)oxy)benzeneHCID 15281122—
EduktLithium bis(trimethylsilyl)amideHCID 57426343—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-oneHCID 9840975—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Place lithium hexamethyldisilazane (2 mL of a 1M solution in tetrahydrofuran, 2 mmol) and tetrahydrofuran (8 mL) under an argon atmosphere and cool to 0° C. Add a solution of 3-(4methoxybenzyloxy)phenylacetylene (0.48 g, 2 mmol) in tetrahydrofuran and stir the brown solution for 45 minutes at 0° C. Add N-methoxy-N-methylbenzamide (0.4 g, 2.4 mmol), remove the cooling bath andstir at room temperature for 1 hour. Partition the mixture between ethyl ether and water, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo to yield an oil. Filter through silica gel and elute with 10% ethyl acetate/hexane to yield a crude solid. Recrystallize (hexane, ethyl ether) to yield 0.26 g (lst crop) and 0.15 g (2nd crop) of the title compound; mp 79°-80 C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05446068
Quelldatensatzuspto-grants-1995_08
ORD IDord-48780852258f42e2936b931423a3798e
Quellennotizuspto-grants-1995_08