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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 272351Erstellt: 26. Oktober 2026

Water → N-[4-[[(E)-3-(4-Isopropylphenyl)-2-propenyl]oxy]-2,3,6-trimethylphenyl]formamide

https://huagongshe.com/reaction/272351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktN-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
Edukt1-[(E)-3-bromo-1-propenyl]-4-isopropylbenzeneHCID 21961313—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[4-[[(E)-3-(4-Isopropylphenyl)-2-propenyl]oxy]-2,3,6-trimethylphenyl]formamideHCID 2196134259,3%

Reaktionsschritte

To a solution of N-(4-hydroxy-2,3,6-trimethylphenyl)formamide (5.20 g, 29.0 mmol) in N,N-dimethylformamide (30 ml) was added at 0° C. under a nitrogen atmosphere sodium hydride (a 60% dispersion in liquid paraffin, 1.39 g, 34.8 mmol) and the resulting mixture was stirred at the same temperature for 10 minutes. To the reaction solution was added 1-[(E)-3-bromo-1-propenyl]-4-isopropylbenzene (9.00 g, 37.7 mmol) 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-hexane to obtain 5.80 g (59% yield) of the title compound. Melting point: 165-167° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456162B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-dfd0ca46395e4a76a44a12a4b2353bcf
Quellennotizuspto-grants-2008_11