HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 1-Cyano-4-(tert-butylsulfonylamino)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-Cyano-4-(tert-butylsulfinyl-amino)piperidine | HCID 23154157 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Cyano-4-(tert-butylsulfonylamino)piperidine | HCID 23154173 | — |
Reaction Steps
Meta-chloroperbenzoic acid (60 mg) was added to the chloroform solution (0.5 mL) containing 1-cyano-4-(tert-butylsulfinyl-amino)piperidine at room temperature, followed by stirring at the same temperature for 16 hrs. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with aqueous saturated sodium hydrogencarbonate and aqueous saturated sodium chloride solutions successively, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound (58 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691860B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-0b2ca38af9214ad18c5c24d5df00a507 |
| Source note | uspto-grants-2010_04 |