HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225406Generated: October 25, 2026
Hydrochloric Acid → HCID 86612198, compound
https://huagongshe.com/reaction/225406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triphenylsulfonium 1,1,3,3,3-pentafluoro-2-benzoyloxypropane-1-sulfonate | HCID 23118490 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86612198 | HCID 86612198 | 85% |
Reaction Steps
In 72 g of methanol was dissolved 34.4 g of triphenylsulfonium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate synthesized in Synthesis Example 10. While stirring under ice cooling, 54.0 g of a 5% sodium hydroxide aqueous solution was added dropwise to the solution at a temperature below 10° C. The reaction solution was aged at the temperature for 4 hours. At a temperature below 10° C., 6.8 g of 12N hydrochloric acid was added to quench the reaction. The methanol was distilled off under vacuum, and 270 g of dichloromethane was added. The organic layer was washed with 40 g of water three times. The organic layer was then concentrated and 60 g of diethyl ether was added to the residue for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 24.3 g (yield 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07556909B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-6f7f33b144804d3d98407aa7de735403 |
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| Source note | uspto-grants-2009_07 |
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