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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091373Generated: November 1, 2026

Triphenylphosphine → HCID 66594811, compound

https://huagongshe.com/reaction/1091373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant1-(4-Hydroxypiperidin-1-yl)ethan-1-oneHCID 10749291—
ReactantHCID 66594479HCID 66594479—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66594811HCID 6659481157.3%

Reaction Steps

Diisopropylazodicarboxylate (40% in toluene, 5.7 g, 11.3 mmol) was added to a solution of (2S)-2-(4-hydroxyphenyl)-4-benzylmorpholine (2.0 g, 7.43 mmol), triphenylphosphine (3.0 g, 11.4 mmol) and 1-acetyl-4-hydroxypiperidin (1.6 g, 11.2 mmol) in tetrahydrofuran (40 ml) at room temperature and the mixture stirred for 10 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography eluting 10-50% ethyl acetate in hexane to furnish (2S)-2-(4-(1-acetylpiperidin-4-yloxy)phenyl)-4-benzylmorpholine (1.68 g, 57%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129377B2
Source datasetuspto-grants-2012_03
ORD IDord-2aaafb3a423c4499b3a54c5d2a7f97cc
Source noteuspto-grants-2012_03