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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707577Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
ReactantDiethyl squarateHCID 123228—
Reactant8-Chloro-dibenz[b,f]-[1,4]oxazepineHCID 838267—
Solvent1,4-DioxaneHCID 31275—
Product3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dioneHCID 15232293—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354746
Source datasetuspto-grants-1994_10
ORD IDord-57f9b35e48a04aa2872b5c7c2667e77f
Source noteuspto-grants-1994_10