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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078029Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3a,7a-dihydro-2,2-dimethyl-1,3-Benzodioxole

https://huagongshe.com/reaction/2078029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5,6-Dibromo-2,2-dimethylhexahydro-2H-1,3-benzodioxoleHCID 12885768—
SolventTolueneHCID 1140—
Product3a,7a-dihydro-2,2-dimethyl-1,3-BenzodioxoleHCID 11768761—

Reaction Steps

The compound obtained in Step (11) was placed in a reaction vessel, and air in the vessel was replaced with nitrogen. After that, the compound was dissolved in dehydrated toluene (116 ml). Distilled DBU (6.0 ml, 40.1 mmol) was added to the solution, and the mixture was refluxed for 6 hours. After the reaction product had been filtrated, sodium hydrogen carbonate was added to the filtrate, and the organic layer was dried over magnesium sulfate, whereby 2,2-dimethyl-3a,7a-dihydrobenzo[1.3]dioxol was obtained. The compound was used in the next reaction without being further purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928221B2
Source datasetuspto-grants-2011_04
ORD IDord-f106c428679c43f78217743b87c6b20e
Source noteuspto-grants-2011_04