Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl sulfide | HCID 8766 | — |
| Reactant | HCID 23081881 | HCID 23081881 | — |
| Product | HCID 131732972 | HCID 131732972 | 85% |
Reaction Steps
Methyl bis(pentafluoroethyl)phosphinate, (C2F5)2P(O)OCH3, (1.77 g; 5.6 mmol) is slowly added dropwise to cooled (0° C.) diphenyl sulfide (1.01 g; 5.4 mmol) in a 25 ml glass flask. The two-phase reaction mixture is warmed and stirred at 45° C. for 17 h. The readily volatile constituents are removed in vacuo (10−3 mbar) at room temperature. Methyldiphenylsulfonium bis(pentafluoroethyl)phosphinate, [CH3S(C6H5)2][(C2F5)2P(O)O], (2.31 g, 4.6 mmol) is isolated as pale-yellow and highly viscous liquid in a yield of 85% and a purity of 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056881B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-642121e00d574549bcda00e228bfb366 |
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| Source note | uspto-grants-2015_06 |
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