HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidine → 4-(2-(Methylsulfinyl)phenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidine | HCID 22622247 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(2-(Methylsulfinyl)phenyl)piperidine | HCID 18700387 | 83.9% |
Reaction Steps
A solution of 1-benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidine (1.66 g) in 8 mL of trifluoroacetic acid was heated to reflux for 45 minutes. At the end of this period, the reaction mixture was evaporated and the residue was treated with toluene. Upon evaporating the solvent, the residue was treated with an additional portion of toluene and the process was repeated. The final residue was dried under reduced pressure and purified by chromatography; elution with dichloromethane:methanol:triethylamine (19:1:1) afforded the named product (0.87 g); MS: 224; NMR: 1.6-2.4 (m, 4), 2.7 (two peaks, 3), 2.9-3.2 (m, 3), 3.3-3.5 (m, 2), 5.3-5.7 (br, 1), 7.4-7.5 (m, 3), 7.9-8.0 (m, 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05654299 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-c30efc5ee7bf4ce7b3bcb7f8bee00e91 |
| Source note | uspto-grants-1997_08 |