HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 424331Erstellt: 25. Oktober 2026
Hydrochloric Acid → Triphenylsulfonium 1,1-difluoro-2-hydroxyethanesulfonate
https://huagongshe.com/reaction/424331
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Triphenylsulfonium 2-pivaloyloxy-1,1-difluoroethanesulfonate | HCID 86632753 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Triphenylsulfonium 1,1-difluoro-2-hydroxyethanesulfonate | HCID 86632756 | 78% |
Reaktionsschritte
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, an aqueous sodium hydroxide solution (40 g sodium hydroxide in 120 g water) was added dropwise at a temperature below 5° C. The reaction solution was allowed to mature 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 three times with 30 g of saturated saline and concentrated. Diisopropyl ether, 1 L, was added to the concentrate for crystallization. The crystals were filtered and dried, obtaining the target compound (PAG1), 187 g (purity 78%, net yield 78%). PAG1 has the following structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08105748B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-d34f9c30aeb84069b05142c4cb9d9f11 |
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| Quellennotiz | uspto-grants-2012_01 |
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