HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene → Methyl rac-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene | HCID 13264175 | — |
| Reactant | Methyl rac-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthalene-2-carboxylate | HCID 20283297 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Methyl rac-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene-2-carboxylate | HCID 20283275 | 81.2% |
Reaction Steps
A mixture of 240 mg (1.1 mmol) of trans-1,2-diacetoxy-1,2-dihydrobenzocyclobutene and 220 mg (1.0 mmol) of methyl rac-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthalene-2-carboxylate in 20 ml of dry xylene was stirred and heated under reflux under an atmosphere of nitrogen for 18 hours. The solution was evaporated to dryness, the yellow residue was stirred with 10 ml of diethyl ether and the mixture was subsequently filtered to give 260 mg (81%) of methyl rac-1,2,3,4,5,12-hexahydro-5,12-dioxonaphthacene-2-carboxylate in the form of a bright yellow solid of melting point 173°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518784 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-cd0c6956a1194751859415a76523431e |
| Source note | uspto-grants-1985_05 |