HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylbenzene → (4-(Tert-butyl)phenyl)(chloromethyl)(phenyl)sulfonium triflate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylbenzene | HCID 7366 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Chloromethyl phenyl sulfoxide | HCID 81624 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-(Tert-butyl)phenyl)(chloromethyl)(phenyl)sulfonium triflate | HCID 86699376 | — |
Reaction Steps
Chloromethyl phenyl sulfoxide (200 mg, 1.29 mmol) of example 21 was dissolved in dry diethyl ether (7.5 mL) under an argon atmosphere. tert-Butyl benzene (0.191 g, 1.1 eq) was added to the previous solution and then the mixture was cooled to a temperature below −60° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.217 mL, 1 eq) was added slowly maintaining the same temperature. The mixture was stirred until the reaction was complete. The orange precipitated triflate salt was quickly filtered at −60° C. affording 0.487 g as red viscous oil after heating at room temperature, which was a mixture by proton NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359294B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-cb5d240bbcea4662ad75e6a1db711fce |
| Source note | uspto-grants-2016_06 |