Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256050Generated: November 1, 2026

1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidine → 4-(2-(Methylsulfinyl)phenyl)piperidine

https://huagongshe.com/reaction/2256050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidineHCID 22622247—
SolventTrifluoroacetic acidHCID 6422—
Product4-(2-(Methylsulfinyl)phenyl)piperidineHCID 1870038783.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654299
Source datasetuspto-grants-1997_08
ORD IDord-c30efc5ee7bf4ce7b3bcb7f8bee00e91
Source noteuspto-grants-1997_08