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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70756Erstellt: 23. Oktober 2026

2,3-Dimethoxy-1,3-butadiene → 3,4-Dimethoxyselenophene

https://huagongshe.com/de/reaction/70756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dimethoxy-1,3-butadieneHCID 19169—
EduktSelenium chlorideHCID 139762—
EduktAcetone cardiceHCID 18522661—
EduktHCID 178418247HCID 178418247—
LösungsmittelHexaneHCID 8058—
Produkt3,4-DimethoxyselenopheneHCID 24886169—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a well stirred solution of 2,3-dimethoxy-1,3-butadiene (1.47 g, 12.9 mmol, (11)) and CH3COONa (2.64 g, 32.25 mmol) in dry hexane (80 mL) at −78° C. (dry ice/acetone bath), under an inert atmosphere, was added a solution of freshly prepared SeCl2 in hexane over a period of 15 min. The resulting yellowish solution was further stirred for 1 h at −78° C. and then removed from the cooling bath and the reaction mixture was brought to room temperature over a period of 2 h and further stirred for 5 h. The reaction mixture was filtered through neutral alumina and washed with hexane. The residue was concentrated to give brown yellow oil. The crude product was purified by flash column chromatography on TLC grade silica gel (Hexane:Ethyl acetate—95:5) to provide DMOS (0.85 g, 35%, (12)) as a white crystalline solid. mp. 43-45° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822635B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-18f9441165df4406b6d2489b4d5df025
Quellennotizuspto-grants-2014_09