Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820652Generated: October 29, 2026

4-Benzyl-2-methyl-6-(trifluoromethyl)morpholin-3-one → 4-Benzyl-cis-2-methyl-6-(trifluoromethyl)morpholine

https://huagongshe.com/reaction/1820652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-2-methyl-6-(trifluoromethyl)morpholin-3-oneHCID 18455591—
ReactantAluminium lithium hydrideHCID 21226445—
Product4-Benzyl-cis-2-methyl-6-(trifluoromethyl)morpholineHCID 58847029—

Reaction Conditions

Temperature60 °C

Reaction Steps

Dry LiAlH4 (797 mg, 21 mmol, Aldrich) is suspended in dry, inhibitor free THF (15 ml) and treated with a solution of 4-benzyl-2-methyl-6-(trifluoromethyl)morpholin-3-one (2.73 g, 10 mmol) in dry, inhibitor free THF (15 ml). The mixture is heated to 60° C. with stirring for 30 minutes. The mixture is diluted with MTBE (25 mL) and quenched sequentially with H2O (0.8 mL), 6.0 M NaOH (0.8 mL) and H2O (2.4 mL). The white slurry is filtered and the inorganic salts were washed with MTBE (200 mL). The solvent is removed by rotary evaporation and the product is purified in 3 portions on Biotage Flash 40M+ cartridges using a 10 minute linear gradient of 3% -10% MTBE in heptane. The products are combined and dried under high vacuum yielding a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605157B2
Source datasetuspto-grants-2009_10
ORD IDord-d5f38d0dbb4f47dbb75b6e50fe5cac6d
Source noteuspto-grants-2009_10