Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799516Generated: November 1, 2026

1-[4-(Phenylmethoxy)phenyl]-4-[4-(trifluoromethoxy)phenoxy]piperidine → SS-3227

https://huagongshe.com/reaction/1799516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[4-(Phenylmethoxy)phenyl]-4-[4-(trifluoromethoxy)phenoxy]piperidineHCID 68483077—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductSS-3227HCID 11653258101.7%

Reaction Steps

After 1-(4-Benzyloxyphenyl)-4-[4-(Trifluoromethoxy)phenoxy]piperidine (20.0 g) and ethyl alcohol (200 mL) was mixed and then (50% wet) 5 w/w % palladium on carbon (1 g) was added. The resulting mixture was stirred under 4 atms of atmosphere of hydrogen at 60-61° C. for 3 hr. The reaction mixture was then cooled to room temperature and was filtered to remove the catalyst followed by concentration in vacuo to give 16.2 g (99.5% yield) of an ivory crystal target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344148B2
Source datasetuspto-grants-2013_01
ORD IDord-cd024d5704554145b51aec56f24e014b
Source noteuspto-grants-2013_01