Basic information Safety Supplier Related

(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE

Basic information Safety Supplier Related

(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Basic information

Product Name:
(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE
Synonyms:
  • (R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE
  • R-(+)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE
  • (4R)-4-phenyl-3-propanoyl-1,3-oxazolidin-2-one
  • (R)-4-Phenyl-3-propionyl-2-oxazolidinone, ee: 97%
  • (R)-4-Phenyl-3-propionyl-2-oxazolidinone,99%e.e.
  • (4R)-4-Phenyl-3-Propionyl-1,3-Oxazolidin-2-One
  • (R)-4-Phenyl-3-propionyloxazolidin-2-one 95+%
  • 2-Oxazolidinone, 3-(1-oxopropyl)-4-phenyl-, (4R)-
CAS:
160695-26-1
MF:
C12H13NO3
MW:
219.24
Mol File:
160695-26-1.mol
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(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Chemical Properties

Melting point:
83.5-84 °C(Solv: hexane (110-54-3); toluene (108-88-3))
Boiling point:
393.1±31.0 °C(Predicted)
Density 
1.223±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-3.13±0.40(Predicted)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
HS Code 
29349990
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(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Usage And Synthesis

Synthesis

79-03-8

90319-52-1

160695-26-1

1. (R)-4-phenyl-2-oxazolidinone (16.3 g, 1.0 eq.) was dissolved in 180 mL of dichloromethane and cooled to 0 °C in an ice bath. 2. Triethylamine (15.2 g, 1.5 eq.) and 4-dimethylaminopyridine (DMAP) (366 mg, 0.03 eq.) were added sequentially with stirring. 3. Propionyl chloride (9.2 g, 1.0 eq.) was added slowly and dropwise, keeping the reaction temperature at 0 °C and continuing to stir for 1 hour. 4. Upon completion of the reaction, the reaction mixture was diluted with methylene chloride and washed sequentially with water and saturated sodium bicarbonate solution. 5. Separate the organic phase and dry with anhydrous sodium sulfate. 6. The solvent was removed by depressurized evaporation to obtain the crude product. 7. The crude product was purified by column chromatography to afford the target compound R-4-phenyl-3-propionyl-2-oxazolidinone (III-a) (20.1 g, 92% yield).

References

[1] Organic Letters, 2011, vol. 13, # 21, p. 5762 - 5765
[2] Patent: CN105085322, 2017, B. Location in patent: Paragraph 0065; 0066; 0067; 0068
[3] Organic Process Research and Development, 2005, vol. 9, # 6, p. 827 - 829
[4] Advanced Synthesis and Catalysis, 2018, vol. 360, # 5, p. 965 - 971

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