HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(2-(Methylsulfinyl)phenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidine | HCID 22622247 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(2-(Methylsulfinyl)phenyl)piperidine | HCID 18700387 | 96% |
Reaction Steps
The product of Step 4 (0.5 g) was treated with trifluoroacetic acid (10 mL) and heated at reflux temperature for 45 minutes. The reaction mixture was cooled, diluted with toluene (40 mL) and evaporated. This procedure was repeated two more times. The residue was treated with CH2Cl2 (70 mL) and adjusted to alkaline pH via addition of NH4OH solution. The organic layer was separated, dried over MgSO4, filtered and evaporated to give 4-(2-methylsulfinylphenyl)piperidine (0.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063926 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-5949296e1be34bedbe3dd516b08dde39 |
| Source note | uspto-grants-2000_05 |