HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → 156324-03-7
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Diphenyl sulfide | HCID 8766 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | Sodium hexafluoroantimonate | HCID 16689647 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 156324-03-7 | HCID 18951198 | — |
Reaction Steps
1 mol of diphenyl sulfide is dissolved in an excess of cyclohexene and and to the solution is added 1 mol of HBF4 (54% etherate) and the mixture is stirred at room temperature. After c. 15 minutes a second phase forms. The product is isolated by addition of ether and dissolved in acetone. Afterwards, sodium hexafluoroantimonate is added to the solution and the resulting cyclohexyldiphenylsulfonium hexafluoroantimonate is precipitated by addition of water. The compound has a melting point of 129° C. and the analytical data obtained are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374697 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-fa7a9f17fecd4757875038f6832f955e |
| Source note | uspto-grants-1994_12 |