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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Morpholinone | HCID 66953 | — |
| Reactant | (6S)-4-benzyl-6-(4-fluorophenyl)morpholin-3-one | HCID 15982164 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-4-Benzyl-2-(4-fluorophenyl)morpholine | HCID 12002488 | 92.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994315B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-cfc8e4972cbe4906bd1deb971334ba69 |
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| Source note | uspto-grants-2011_08 |
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