HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cumene → (Chloromethyl)(isopropylphenyl)(phenyl)sulfonium triflate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cumene | HCID 7406 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Chloromethyl phenyl sulfoxide | HCID 81624 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (Chloromethyl)(isopropylphenyl)(phenyl)sulfonium triflate | HCID 86699374 | — |
Reaction Steps
Chloromethyl phenyl sulfoxide (170 mg, 1.1 mmol) of example 21 was dissolved in dry diethyl ether (5 mL) under an argon atmosphere. Cumene (145 mg, 1.1 eq) was added to the previous solution and the mixture was cooled to a temperature below −60° C. After stabilizing the temperature, trifluoromethanesulfonic anhydride (0.184 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 0.399 g as orange 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-4597a8b7c2264768aebf554c18d360d3 |
| Source note | uspto-grants-2016_06 |