Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186419Generated: November 2, 2026

HCID 67401817, compound → HCID 67402546, compound

https://huagongshe.com/reaction/1186419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67401817HCID 67401817—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 67402546HCID 6740254699%

Reaction Steps

Ten percent palladium/carbon (170 mg) was suspended in ethanol (5.0 mL). To this, an ethanol solution (25 mL) of 1-benzyloxycarbonyl-4-[2,2,2-trifluoro-1-(triethylsiloxy)-ethyl]piperidine (1.69 g, 3.92 mmol) was added and the mixture was stirred under a hydrogen atmosphere at room temperature for 2.5 hours. The reaction mixture was filtered through Celite and the solvent was evaporated off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform) to give 4-[2,2,2-trifluoro-1-(triethylsiloxy)ethyl]piperidine (1.15 g, yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-caea788756ab4cdfb567fe3950e7f54d
Source noteuspto-grants-2014_03