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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108030Generated: October 30, 2026

Trifluoroacetic acid → 4-(2-(Methylsulfinyl)phenyl)piperidine

https://huagongshe.com/reaction/1108030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Benzyloxycarbonyl-4-(2-methylsulfinylphenyl)piperidineHCID 22622247—
SolventTolueneHCID 1140—
Product4-(2-(Methylsulfinyl)phenyl)piperidineHCID 1870038796%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063926
Source datasetuspto-grants-2000_05
ORD IDord-5949296e1be34bedbe3dd516b08dde39
Source noteuspto-grants-2000_05