HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249856Generated: October 31, 2026
Aluminium lithium hydride → (3R)-4-Benzyl-3-methylmorpholine
https://huagongshe.com/reaction/249856
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 51357134 | HCID 51357134 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3R)-4-Benzyl-3-methylmorpholine | HCID 51357135 | 97.8% |
Reaction Steps
A solution of (R)-4-benzyl-5-methylmorpholine-3-one (3.0 g, 14.22 mmol) in THF (10 mL) was added dropwise at 0° C. to a solution of lithium aluminum hydride (1.0 M solution in THF, 28.5 mL, 28.5 mmol) in THF (10 mL). The ice bath was removed and the reaction mixture was heated at reflux for 18 h. The reaction was cooled in an ice-bath and excess hydride reagent was quenched by careful, dropwise addition of H2O (5 mL), 15% sodium hydroxide (5 mL) and H2O (15 mL). The resulting mixture was stirred at room temperature for 1 h and the reaction mixture was filtered through a pad of Celite and the pad rinsed with EtOAc (100 mL). The filtrate was washed with saturated brine solution, dried (Na2SO4), filtered and concentrated under reduced pressure to provide (R)-4-benzyl-3-methylmorpholine (2.66 g, 95%) as a red oil. 1H NMR and MS consistent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863271B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-6fed043447574939af6f5a2cf375c9ca |
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| Source note | uspto-grants-2011_01 |
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