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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424422Generated: October 29, 2026

(S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)-4-((R)-1-phenylethyl)morpholine → (2S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)morpholine

https://huagongshe.com/reaction/424422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)-4-((R)-1-phenylethyl)morpholineHCID 66703943—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(2S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)morpholineHCID 6670400295%

Reaction Conditions

Temperature50 °C

Reaction Steps

A 300-ml flask containing a solution of (S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)-4-((R)-1-phenylethyl)morpholine (7.27 g, 19.07 mmol) and 10% palladium on carbon (3.0 g) in ethanol (30 ml) was charged with hydrogen. The reaction mixture was stirred vigorously at 50° C. for 10 hours. The catalyst was filtered off with a Celite pad, and the filtrate was concentrated under reduced pressure to yield (2S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)morpholine (4.95 g, 95%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-1e77c92184e04ea2b195d40fb0c901e4
Source noteuspto-grants-2012_01