HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792323Generated: November 4, 2026
HCID 22033137, compound → HCID 22033384, compound
https://huagongshe.com/reaction/1792323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22033137 | HCID 22033137 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22033384 | HCID 22033384 | 81% |
Reaction Steps
To a solution of (3RS,4RS)-7-hydroxy-3-methyl-4-[9-(4,4,5,5,5-pentafluoropentylthio)nonyl]-3-(4-pyridyl)chroman (6.1 mg, 0.011 mmol) in tetrahydrofuran (0.5 ml) was added under ice-cooling a solution of Oxone® (monopersulfate compound; DuPont product) (3.4 mg, 0.0055 mmol) in water (0.5 ml), which was then stirred for 5 hours. After the reaction was completed, the reaction solution was extracted with ethyl acetate and washed with saturated saline solution. The organic layer was dried over magnesium sulfate, and the solvent was removed under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate) to give (3RS,4RS)-7-hydroxy-3-methyl-4-[9-(4,4,5,5,5-pentafluoropentylsulfinyl)nonyl]-3-(4-pyridyl)chroman (5.1 mg, yield 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07074819B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-2ba87f94156c4f3bb435ba83a2a70596 |
|---|
| Source note | uspto-grants-2006_07 |
|---|