HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl sulfide → Sulfonium, triphenyl-, hexafluoroarsenate(1-) (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl sulfide | HCID 8766 | — |
| Reactant | Iodonium, diphenyl-, hexafluoroarsenate(1-) (1:1) | HCID 2737135 | — |
| Catalyst | Cupric benzoate | HCID 164650 | — |
| Product | Sulfonium, triphenyl-, hexafluoroarsenate(1-) (1:1) | HCID 93839 | 97% |
Reaction Steps
A mixture of 11.75 parts of diphenyliodonium hexafluoroarsenate, 4.065 parts of diphenyl sulfide and 0.2 part of copper benzoate was heated with stirring at a temperature of 120°-125° C. for 3 hours. The mixture was then poured while it was hot into a container whereupon the product crystallized. The product was extracted three times with diethylether and then air dried. There was obtained a 97% yield of triphenylsulfonium hexafluoroarsenate. The triphenylsulfonium hexafluoroarsenate product had a melting point of 195°-197° C. after it was further recrystallized from 95% ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04407759 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-0feac6e6727a472f81132d3655c5ea18 |
| Source note | uspto-grants-1983_10 |