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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)-4-((R)-1-phenylethyl)morpholine | HCID 66703943 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2S)-2-(4-(N-cyclohexyl-N-methylamino)phenyl)morpholine | HCID 66704002 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1e77c92184e04ea2b195d40fb0c901e4 |
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| Source note | uspto-grants-2012_01 |
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