HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571155Generated: November 1, 2026
Triphenylsulfonium Bromide → Triphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate
https://huagongshe.com/reaction/571155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylsulfonium Bromide | HCID 11984010 | — |
| Reactant | Triethylammonium 1,1-difluoro-2-(methacryloyloxy)ethanesulfonate | HCID 86660800 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Triphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate | HCID 86648110 | 87% |
Reaction Steps
A 50 mL reactor was charged with the triethylammonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate aqueous solution obtained by the 3rd step, and a solution of 3.18 g (8.9 millimoles) of triphenylsulfonium bromide and 20 g of chloroform, followed by 3 hours of stirring at room temperature. Subsequently, an organic layer was separated, and the thus obtained organic layer was rinsed with 20 g of water four times. Subsequently, it was rinsed with 20 g of diisopropyl ether three times and then a volatile component was distilled off, thereby obtaining 3.92 g of a target triphenylsulfonium 1,1-difluoro-2-(2-methyl-acryloyloxy)-ethane-1-sulfonate. It exhibited a purity of 97% at this time, and a yield of 87% taken over from the 3rd step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024058B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-7a6d1b98f67a4b15876d1ce5bb9dfedd |
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| Source note | uspto-grants-2015_05 |
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