ChemicalBook--->CAS DataBase List--->1260672-03-4

1260672-03-4

1260672-03-4 Structure

1260672-03-4 Structure
IdentificationBack Directory
[Name]

5-phenylMorpholin-3-one
[CAS]

1260672-03-4
[Synonyms]

5-phenyl-3-morpholinone
3-Morpholinone, 5-phenyl-
[Molecular Formula]

C10H11NO2
[MDL Number]

MFCD18250283
[MOL File]

1260672-03-4.mol
[Molecular Weight]

177.2
Chemical PropertiesBack Directory
[Boiling point ]

401.9±45.0 °C(Predicted)
[density ]

1.149±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.66±0.40(Predicted)
[Appearance]

Light brown to brown Solid
Spectrum DetailBack Directory
[Spectrum Detail]

5-phenylMorpholin-3-one(1260672-03-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Acetamide, 2-chloro-N-(2-hydroxy-1-phenylethyl)-, (R)-

94193-77-8

5-phenylMorpholin-3-one

1260672-03-4

General procedure for the synthesis of 5-phenylmorpholin-3-one from the compound (CAS:94193-77-8): crude 2-chloro-N-(2-hydroxy-1-phenylethyl)acetamide (3 g, 14.04 mmol) was dissolved in anhydrous tetrahydrofuran (THF, 40 mL) and the reaction mixture was cooled to 0 °C. Sodium hydride (NaH, 0.842 g, 35.1 mmol) was added in two portions, followed by slow warming of the reaction mixture to room temperature. Upon completion of the reaction, the reaction was quenched by slow addition of 50% THF/water solution followed by dilution with ethyl acetate (EtOAc). The organic layer was washed sequentially with aqueous sodium bicarbonate (NaHCO3), water and brine. The organic phases were combined and purified by fast column chromatography (eluent: 30-100% EtOAc/heptane gradient) to afford the target product 5-phenylmorpholin-3-one (2.25 g, 90% yield). Liquid chromatography-mass spectrometry (LC/MS) analysis showed the following results: retention time (Rt) = 0.39 min (Table 1, method f); mass spectrum (MS) m/z: 219 ([M+H+MeCN]+).

[References]

[1] Patent: WO2016/168641, 2016, A1. Location in patent: Page/Page column 145; 146
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