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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271911Generated: November 3, 2026

Aluminium lithium hydride → (2S,6S)-4-Benzyl-2,6-dimethylmorpholine

https://huagongshe.com/reaction/1271911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
Reactant[(2S,6S)-2,6-Dimethylmorpholin-4-yl](phenyl)methanoneHCID 67088332—
SolventTetrahydrofuranHCID 8028—
Product(2S,6S)-4-Benzyl-2,6-dimethylmorpholineHCID 11183342—

Reaction Conditions

Temperature55 °C

Reaction Steps

(2S,6S)-4-benzoyl-2,6-dimethylmorpholine (759 mg, 3.46 mmol) is dissolved in anhydrous THF (40 mL) and treated with LiAlH4 (1.0M in THF, 6.9 mL, Aldrich). The mixture is stirred with heating at 55° C. for 18 hours. An additional equivalent of LiAlH4 is added and the mixture is stirred with heating at 55° C. for an additional 6 hours. The reaction is quenched by adding water (0.4 mL) followed by 6.0M NaOH (0.4 mL) followed by water (1.2 mL). The white slurry is diluted with Et2O and filtered. The inorganic salts are washed with and additional portion of Et2O and the combined ethereal washes are dried over Na2SO4. The product is purified on a Biotage Flash 40M+ using a 15% Et2O in pentane as eluent. The product containing fractions are pooled and the solvent is removed by rotary evaporation. The product is dried under vacuum yielding a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208490B2
Source datasetuspto-grants-2007_04
ORD IDord-1efb4e890e274133bf0c8288894d3326
Source noteuspto-grants-2007_04