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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1757510Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1757510

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Methoxy-N-methylbenzamideHCID 569575—
Edukt3-(4-(Dimethylamino)benzyloxy)phenylacetyleneHCID 19388226—
EduktLithium bis(trimethylsilyl)amideHCID 57426343—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-oneHCID 19388218—

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-(4-(dimethylamino)benzyloxy)phenylacetylene (0.51 g, 2 mmol) in tetrahydrofuran and stir the 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. Purifyby silica gel chromatography to give the title compound. Alternatively, compounds of formula (1) can be prepared according to the procedure set forth in Scheme B, wherein all substituents, unless otherwise indicated, are previously described. ##STR3##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05446068
Quelldatensatzuspto-grants-1995_08
ORD IDord-811a5c27251840fcad575856719bd0b2
Quellennotizuspto-grants-1995_08