Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 58495647 | HCID 58495647 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 58495697 | HCID 58495697 | 94% |
Reaction Steps
Dissolve 4-cyclohexylthio-benzonitrile (1.17 g, 5.4 mmol) in acetone (10 mL) and add water until the sulfide starts to come out of solution. Then add a drop of acetone to rehomogenize the solution. Cool the mixture to 0° C. and then add oxone (4.2 g, 6.73 mmol) in one portion while stirring vigorously at 0° C. for h. Concentrate in vacuo, take up the residue in DCM and filter the suspension through a frit. Concentrate in vacuo to obtain the desired intermediate (1.27 g, 94%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08680091B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-50e5346b5b4a499e8d1f91ae7e2f8546 |
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| Source note | uspto-grants-2014_03 |
|---|