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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647653Generated: October 29, 2026

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

https://huagongshe.com/reaction/647653

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-1,2-Diacetoxy-1,2-dihydrobenzocyclobuteneHCID 13264175—
ReactantRac-3-acetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,8-hexahydro-5,8-dioxonaphthaleneHCID 20283301—
SolventTolueneHCID 1140—
ProductRac-3,6,11-triacetoxy-3-acetyl-1,1-ethylenedioxy-1,2,3,4,5,5a,6,11,11a,12-decahydro-5,12-dioxonaphthaceneHCID 2028329142.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409391
Source datasetuspto-grants-1983_10
ORD IDord-1d76038ede144bd09d0d2999585f9c53
Source noteuspto-grants-1983_10