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HRID 29082Erstellt: 24. Oktober 2026

2,6-Dibromopyridine → n-[1-Eth-(z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromide

https://huagongshe.com/de/reaction/29082

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-DibromopyridineHCID 12274—
Edukt4,4,N-Trimethoxy-N-methylbutyramideHCID 59788083—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produktn-[1-Eth-(z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromideHCID 8723332374,9%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

To a suspension of 2,6-dibromopyridine(8.1 g, 34.03 mmol) in 80 mL of ether at −70° C., is added BuLi(12.3 mL, 26.17 mmol, 2.5 M in Hexane) in on portion. After stirring at −70° C. for 5 min, 4,4,N-Trimethoxy-N-methyl-butyramide(5.0 g, 26.17 mmol) is added to the solution dropwise. After stirring at −70° C. for 1.5 hr, the reaction mixture is quenched with 120 mL of water and extracted with 3×130 mL of EtOAc. The combined organic layers is concentrated and purified by chromatography(Hexane/EtOAc:70/30) to give N-[1-Eth-(Z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]-acrylimidoyl bromide(5.96 g, 60.5%) as light yellow liquid. M/Z=288.0

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419975B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-4fd606995a9a445d89b0c7983409a85d
Quellennotizuspto-grants-2008_09