HuagongsheHuagongshe Chemistry Print Report · For research reference only
trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene → Rac-3,6,11-triacetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,5a,6,11,11a,12-decahydro-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 | Toluene | HCID 1140 | — |
| Product | Rac-3,6,11-triacetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,5a,6,11,11a,12-decahydro-5,12-dioxonaphthacene | HCID 20283291 | 42.3% |
Reaction Steps
A solution of 110 mg (0.5 mmol) of trans-1,2-diacetoxy-1,2-dihydrobenzocyclobutene and 112 mg (0.35 mmol) of rac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthalene in 10 ml of toluene was stirred and heated under reflux for 3 hours under an atmosphere of nitrogen. The solution was evaporated and the resulting yellow gum was crystallized from diethyl ether to yield 80 mg (42%) of rac-3,6,11-triacetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,5a,6,11,11a,12-decahydro-5,12-dioxonaphthacene in the form of a pale yellow solid of melting point 133°-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04409391 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-1d76038ede144bd09d0d2999585f9c53 |
| Source note | uspto-grants-1983_10 |