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HRID 1707577作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenyl EtherHCID 7583—
反応物Diethyl squarateHCID 123228—
反応物8-Chloro-dibenz[b,f]-[1,4]oxazepineHCID 838267—
溶媒1,4-DioxaneHCID 31275—
生成物3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dioneHCID 15232293—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05354746
出典データセットuspto-grants-1994_10
ORD IDord-57f9b35e48a04aa2872b5c7c2667e77f
出典メモuspto-grants-1994_10