HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 5,6-Dibromo-2,2-dimethylhexahydro-2H-1,3-benzodioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | 4,5-Dibromo-1,2-cyclohexanediol | HCID 12885764 | — |
| Product | 5,6-Dibromo-2,2-dimethylhexahydro-2H-1,3-benzodioxole | HCID 12885768 | — |
Reaction Steps
The compound obtained in Step (10) (20.6 g, 75.62 mmol) was placed in a reaction vessel, and air in the vessel was replaced with nitrogen. 2,2-dimethoxypropane (12.92 ml) and p-toluenesulfonic acid (0.9 g) were added to the vessel, and the mixture was stirred for 3 hours. After the completion of the reaction had been confirmed, the mixture was filtrated through activated alumina, and the filtrate was concentrated under reduced pressure, whereby 5,6-dibromo-2,2-dimethylhexahydro-1,3-benzodioxol was obtained (17.1 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658459B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-db21b43657454ed49894744823a85fd0 |
| Source note | uspto-grants-2014_02 |