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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16391Generated: October 30, 2026

1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanone → 2-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholine-3-yl]propane-2-ol

https://huagongshe.com/reaction/16391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanoneHCID 67370747—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Product2-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholine-3-yl]propane-2-olHCID 67373384—

Reaction Steps

To a solution of 1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholine-3-yl]ethanone (529 mg) in tetrahydrofuran (25 mL) was, under a nitrogen atmosphere, dropwise added methylmagnesium bromide (0.97 M tetrahydrofuran solution, 4.63 mL) at 0° C. The resultant solution was stirred for 1 hour at the same temperature, and then diluted with aqueous ammonium chloride and ethyl acetate. The organic layer was partitioned, washed with brine, and then dried over anhydrous magnesium sulfate. Solvent was removed by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (heptane/ethyl acetate), to thereby obtain the titled compound (330 mg). The physical properties of this crude product were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737141B2
Source datasetuspto-grants-2010_06
ORD IDord-7a4bb6e137424f54a88c761334c3e19e
Source noteuspto-grants-2010_06