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HRID 1707577Erstellt: 25. Oktober 2026

Diphenyl Ether → 3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dione

https://huagongshe.com/reaction/1707577

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphenyl EtherHCID 7583—
EduktDiethyl squarateHCID 123228—
Edukt8-Chloro-dibenz[b,f]-[1,4]oxazepineHCID 838267—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dioneHCID 15232293—

Reaktionsschritte

A mixture of 8-chloro-dibenz[b,f][1,4]oxazepine (2 g), 3,4-diethoxy-3-cyclobutene-1,2-dione (5 g), diphenylether (2 g) and dioxane (10 mL) was heated to reflux. After 2 hours, most of the dioxane was removed in vacuo and the precipitated title compound (0.75 g) was collected by filtration as yellow solid. The filtrate was treated with cold methanol when more of the title compound (1.2 g) precipitated. This material was used in Example 6 without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05354746
Quelldatensatzuspto-grants-1994_10
ORD IDord-57f9b35e48a04aa2872b5c7c2667e77f
Quellennotizuspto-grants-1994_10