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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671478Generated: November 1, 2026

3-Morpholinone → (S)-4-Benzyl-2-(4-fluorophenyl)morpholine

https://huagongshe.com/reaction/1671478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MorpholinoneHCID 66953—
Reactant(6S)-4-benzyl-6-(4-fluorophenyl)morpholin-3-oneHCID 15982164—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-Benzyl-2-(4-fluorophenyl)morpholineHCID 1200248892.5%

Reaction Steps

To a solution of (6S)-6-(4-fluorophenyl)-4-(benzyl)morpholin-3-one (1.16 g) in tetrahydrofuran (10 mL) was added dropwise over 15 min a solution of sodium bis(2-methoxyethoxy)aluminum hydride (70% in toluene, 3.2 mL, 11.4 mmol) in tetrahydrofuran (5 ml) at 65° C., and the reaction mixture was refluxed over 1.5 hrs. After HPLC analysis to confirm a disappearance of the morpholin-3-one, the reaction was quenched by addition of water (0.6 mL), 15% aqueous sodium hydroxide solution (0.6 mL) and water (1.8 mL) at 0° C. The reaction mixture was filtered and the filtrate was concentrated. To the residue was added ethyl acetate and wash successively with 15% aqueous sodium hydroxide solution and water. The solvent was evaporated to give (2S)-2-(4-fluorophenyl)-4-(benzyl)morpholine (1.02 g, 92% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994315B2
Source datasetuspto-grants-2011_08
ORD IDord-cfc8e4972cbe4906bd1deb971334ba69
Source noteuspto-grants-2011_08