Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734763Generated: October 31, 2026

1-Benzyl-4-(trifluoromethyl)piperidin-4-ol → 4-(Trifluoromethyl)-4-piperidinol

https://huagongshe.com/reaction/734763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(trifluoromethyl)piperidin-4-olHCID 23003702—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Trifluoromethyl)-4-piperidinolHCID 17951321—

Reaction Steps

A suspension of 6.48 g (25.00 mmol) of 1-benzyl-4-trifluoromethylpiperidin-4-ol and 810 mg Pd/C (10%) in 100 mL of MeOH was hydrogenated at RT and 3 bar hydrogen pressure for 17 hours. The catalyst was filtered off and the filtrate evaporated down in vacuo. Yield: 4.22 g (quant. yield); C6H10F3NO (M=169.145); calc.: molpeak (M+H)+: 170; found: molpeak (M+H)+: 17; Rf value: 0.00 (silica gel, cyc/EtOAc 2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-ab68702b99324b55b38f6f38ef6bd6e7
Source noteuspto-grants-2009_09