HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → 3a,7a-dihydro-2,2-dimethyl-1,3-Benzodioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5,6-Dibromo-2,2-dimethylhexahydro-2H-1,3-benzodioxole | HCID 12885768 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3a,7a-dihydro-2,2-dimethyl-1,3-Benzodioxole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928221B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-f106c428679c43f78217743b87c6b20e |
| Source note | uspto-grants-2011_04 |