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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173584Generated: October 31, 2026

Methyl morpholine oxide → benzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1173584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 59556882HCID 59556882—
CatalystHCID 178419074HCID 178419074—
SolventAcetonitrileHCID 6342—
Productbenzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylateHCID 5955693389%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of benzyl(2S,3S)-3-hydroxy-2-methylpyrrolidine-1-carboxylate (20.5 g) in acetonitrile (150 mL) were added powdery molecular sieves 4A (25 g) and 4-methylmorpholine-N-oxide (20.4 g). After cooling to 0° C., tetra-n-propylammonium perruthenate (3.0 g) was added, and the mixture was stirred at 0° C. for 1 hr, and at room temperature for 18 hr. The reaction mixture was concentrated under reduced pressure, and the residue was suspended in ethyl acetate. Insoluble materials were filtered through Hyflo Super-Cel. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1→2/1) to give the title compound as a colorless oil (yield: 18.0 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834051B2
Source datasetuspto-grants-2010_11
ORD IDord-c96cd6d7db6740309029186cb180d7dd
Source noteuspto-grants-2010_11