HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Cyclohexadiene → 5,6-Di(benzenesulfonyl)bicyclo[2.2.2]oct-2-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Cyclohexadiene | HCID 11605 | — |
| Reactant | trans-1,2-Bis(phenylsulfonyl)ethylene | HCID 5367099 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5,6-Di(benzenesulfonyl)bicyclo[2.2.2]oct-2-ene | HCID 12778411 | 104.4% |
Reaction Steps
A mixed solution of 3.16 g (39.5 mmol) of 1,3-cyclohexadiene, 10.5 g (34.1 mmol) of trans-1,2-bis(phenylsulfonyl)ethylene, and 200 ml of toluene was refluxed for 7 hours. Then, the mixed solution was cooled and concentrated under reduced pressure to yield a reaction mixture. The reaction crude product was recrystallized (chloroform/hexane) to yield 5,6-bis(phenylsulfonyl)-bicyclo[2,2,2]octa-2-ene (13.8 g, 35.6 mmol, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07394096B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-71bc67b0a45d4c69999fb7b722b4ffa5 |
| Source note | uspto-grants-2008_07 |