HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene → Rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene | HCID 13264175 | — |
| Reactant | Rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthalene | HCID 20283301 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene | HCID 20283306 | 57% |
Reaction Steps
A mixture of 165 mg (0.75 mmol) of trans-1,2-diacetoxy-1,2-dihydrobenzocyclobutene and 160 mg (0.50 mmol) of rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthalene [prepared as described in Example 7(A)] in 15 ml of xylene was stirred and heated under reflux under an atmosphere of nitrogen for 16 hours. The solution was evaporated to dryness and the yellow residue was stirred with 5 ml of diethyl ether and filtered to give 119 mg (57%) of rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene in the form of a bright yellow solid of melting point 232°-236° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04409391 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-d663babb7d8344d387756e92242b4ead |
| Source note | uspto-grants-1983_10 |