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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 272313Erstellt: 26. Oktober 2026

Water → N-[2,3,6-Trimethyl-4-[[2-methyl-3-(4-methylphenyl)-2-propenyl]oxy]phenyl]formamide

https://huagongshe.com/reaction/272313

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktN-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
Edukt1-(3-Bromo-2-methyl-1-propenyl)-4-methylbenzeneHCID 68706538—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[2,3,6-Trimethyl-4-[[2-methyl-3-(4-methylphenyl)-2-propenyl]oxy]phenyl]formamideHCID 7385674944%

Reaktionsschritte

To a solution of N-(4-hydroxy-2,3,6-trimethylphenyl)formamide (9.31 g, 52.0 mmol) in N,N-dimethylformamide (120 ml) was added at 0° C. under nitrogen atmosphere sodium hydride (a 60% dispersion in liquid paraffin, 2.11 g, 52.8 mmol) and the resulting mixture was stirred at the same temperature for 10 minutes. To the reaction solution was added a solution of 1-(3-bromo-2-methyl-1-propenyl)-4-methylbenzene (12.48 g, 55.44 mmol) in N,N-dimethylformamide (20 ml) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added into the reaction solution and the product was extracted twice with ethyl acetate. The combined extracts were washed with water, dried on magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was crystallized from ethyl acetate-isopropyl ether to obtain 7.34 g (44% yield) of the title compound. Melting point: 167-169° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456162B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-bc3405fed0b2487f82414ca9ae7a2da6
Quellennotizuspto-grants-2008_11