Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylsulfonium chloride | HCID 61343 | — |
| Reactant | HCID 86648109 | HCID 86648109 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86648108 | HCID 86648108 | 92.5% |
Reaction Steps
A 300-mL reaction vessel was charged with 31.85 g (purity: 47%, 48.0 mmol) of sodium cyclohexylcarbamic acid-2,2-difluoroethylsulfonate, 15.8 g (52.9 mmol) of triphenylsulfonium chloride, 170 g of water and 30 g of chloroform. The resulting solution was stirred for 4 hours at room temperature and separated into two phases. The aqueous phase was extracted with chloroform. The thus-obtained organic phases were combined together. The combined organic phase faction was washed six times with water, subjected to concentration, washed three times with diisopropyl ether, and then, dried, thereby yielding 24.5 g of triphenylsulfonium cyclohexylcarbamic acid-2,2-difluoroethylsulfonate as a target product. The purity of the product was 76%; and the yield of the product was 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283106B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-eb64b11c63fe47aa9deb860572d20034 |
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| Source note | uspto-grants-2012_10 |
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