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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856067Generated: October 30, 2026

HCID 23081284, compound → HCID 23081307, compound

https://huagongshe.com/reaction/856067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23081284HCID 23081284—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 23081307HCID 2308130794.4%

Reaction Steps

A mixture of tert-butyl N-(1-benzylpiperidin-4-yl)-N-[2-(4-trifluoromethylphenyl)ethyl]carbamate (0.437 g, 0.944 mmol) prepared in Reference Example 120 and 20% palladium hydroxide/carbon (100 mg) in ethanol (20 ml) was stirred at room temperature under an atmospheric pressure of hydrogen. The reaction mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure to afford tert-butyl N-(piperidin-4-yl)-N-[2-(4-trifluoromethylphenyl)ethyl]carbamate (0.332 g, yield 94%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-2dcc78af1d04498f93c33e92623f1e1b
Source noteuspto-grants-2007_08