Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463474Generated: October 29, 2026

trans-1,2-Diacetoxy-1,2-dihydrobenzocyclobutene → Methyl rac-1',2',3',4',5',12'-hexahydro-5',12'-dioxospiro[1,3-dithiolane-2,4'-naphthacene]-2'-carboxylate

https://huagongshe.com/reaction/463474

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttrans-1,2-Diacetoxy-1,2-dihydrobenzocyclobuteneHCID 13264175—
ReactantMethyl rac-1',2',3',4',5',8'-hexahydro-5',8'-dioxospiro[1,3-dithiolane-2,4'-naphthalene]-2'-carboxylateHCID 20283295—
SolventO-XyleneHCID 7237—
ProductMethyl rac-1',2',3',4',5',12'-hexahydro-5',12'-dioxospiro[1,3-dithiolane-2,4'-naphthacene]-2'-carboxylateHCID 2028327960.3%

Reaction Steps

A mixture of 70 mg (0.32 mmol) of trans-1,2-diacetoxy-1,2-dihydrobenzocyclobutene and 66 mg (0.21 mmol) of methyl rac-1',2',3',4',5',8'-hexahydro-5',8'-dioxospiro[1,3-dithiolane-2,4'-naphthalene]-2'-carboxylate [prepared as described in Example 2(A)] in 5 ml of xylene was stirred and heated under reflux under an atmosphere of nitrogen for 23 hours. The mixture was evaporated to dryness and the residue was stirred with 5 ml of diethyl ether and then filtered to give 52 mg (60%) of methyl rac-1',2',3',4',5',12'-hexahydro-5',12'-dioxospiro[1,3-dithiolane-2,4'-naphthacene]-2'-carboxylate in the form of a bright yellow solid of melting point 216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518784
Source datasetuspto-grants-1985_05
ORD IDord-753003ce7972440eb405c8310e51253d
Source noteuspto-grants-1985_05