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

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Products Intro: Product Name:(R)-4-Phenyl-3-propionyloxazolidin-2-one
CAS:160695-26-1
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Products Intro: Product Name:(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE
CAS:160695-26-1
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CAS:160695-26-1
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Products Intro: Product Name:(4R)-4-phenyl-3-propanoyl-oxazolidin-2-one
CAS:160695-26-1
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Products Intro: Product Name:(R)-4-Phenyl-3-propionyl-2-oxazolidinone
CAS:160695-26-1
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(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE manufacturers

(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
EINECS:
Product Categories:
Mol File:160695-26-1.mol
(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Structure
(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)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36
HS Code 29349990
MSDS Information
(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Usage And Synthesis
Synthesis
Propionyl chloride

79-03-8

(R)-(-)-4-Phenyl-2-oxazolidinone

90319-52-1

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

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
(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE Preparation Products And Raw materials
Raw materialsPropionyl chloride-->(R)-(-)-4-Phenyl-2-oxazolidinone-->Propionic-2,3-14C1 acid (8CI)-->4-Dimethylaminopyridine-->Triethylamine-->Dichloromethane
Tag:(R)-4-PHENYL-3-PROPIONYL-2-OXAZOLIDINONE(160695-26-1) Related Product Information
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