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HRID 1757502Erstellt: 26. Oktober 2026

Pyridine → N,3,4,5-tetramethoxy-N-methyl-Benzamide

https://huagongshe.com/reaction/1757502

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
LösungsmittelEthanolHCID 702—
ProduktN,3,4,5-tetramethoxy-N-methyl-BenzamideHCID 26753597,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Dissolve 3,4,5-trimethoxybenzoyl chloride (2.3 g, 10 mmol) and N,O-dimethylhydroxylamine hydrochloride (1.10 g, 11 mmol) in ethanol-free chloroform at room temperature. Cool the solution to 0° C. and add pyridine (1.85 g, 22 mmol). Stir at ambient temperature for 1 hour and evaporate the solvent in vacuo. Partition the residue between aqueous sodium chloride and a 1:1 mixture of ethyl ether and methylene chloride. Separate the organic phase, dry (Na2SO4), and evaporate the solvent in vacuo to yield an oil. Filter the oil through silica gel eluting with 65% ethyl acetate/hexane to yield 2.5 g of N-methoxy-N-methyl-(3,4,5-trimethoxy)benzamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05446068
Quelldatensatzuspto-grants-1995_08
ORD IDord-b069b36463db499283f63e20862fef94
Quellennotizuspto-grants-1995_08