HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640376Generated: October 31, 2026
Hydrochloric Acid → Triphenylsulfonium 1,1-difluoro-2-hydroxyethanesulfonate
https://huagongshe.com/reaction/1640376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triphenylsulfonium 2-pivaloyloxy-1,1-difluoroethanesulfonate | HCID 86632753 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Triphenylsulfonium 1,1-difluoro-2-hydroxyethanesulfonate | HCID 86632756 | 78% |
Reaction Steps
In 760 g of methanol was dissolved 243.5 g (0.48 mole) of triphenylsulfonium 2-pivaloyloxy-1,1-difluoroethane-sulfonate. To this solution under ice cooling, a sodium hydroxide aqueous solution (40 g sodium hydroxide in 120 g water) was added dropwise at a temperature below 5° C. The reaction solution was aged at room temperature for 8 hours, and dilute hydrochloric acid (99.8 g 12N hydrochloric acid in 200 g water) was added thereto at a temperature below 10° C. to quench the reaction. The methanol was distilled off in vacuum. To the residue was added 1,000 g of dichloromethane. The organic layer was washed with 30 g of saturated saline three times and concentrated. Diisopropyl ether, 1 L, was added to the concentrate for crystallization. The crystals were filtered and dried, obtaining the target compound. 187 g (purity 78%, net yield 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08114571B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-d1927723b2f044838e3d91cb61b074f9 |
|---|
| Source note | uspto-grants-2012_02 |
|---|