HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl Ether → 3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Diethyl squarate | HCID 123228 | — |
| Reactant | 8-Chloro-dibenz[b,f]-[1,4]oxazepine | HCID 838267 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(8-Chloro-dibenz[b,f][1,4]oxazepin-10(11H)-yl)-4-ethoxy-3-cyclobutene-1,2-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05354746 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-57f9b35e48a04aa2872b5c7c2667e77f |
| Source note | uspto-grants-1994_10 |