Basic information Safety Supplier Related

1-(4-FLUOROPHENYL)-2-PYRROLIDINONE

Basic information Safety Supplier Related

1-(4-FLUOROPHENYL)-2-PYRROLIDINONE Basic information

Product Name:
1-(4-FLUOROPHENYL)-2-PYRROLIDINONE
Synonyms:
  • BUTTPARK 32\07-63
  • 1-(4-FLUOROPHENYL)-2-PYRROLIDINONE
  • 1-(4-Fluorophenyl)-2-pyrrolidone 97%
  • 1-(4-Fluorophenyl)-2-pyrrolidone97%
  • 1-(4-Fluorophenyl)pyrrolidin-2-one
  • 1-(4-FLUOROPHENYL)-2-PYRROLIDINONE 99+%
  • 1-(4-Fluorophenyl)-2-oxopyrrolidine, 1-Fluoro-4-(2-oxopyrrolidin-1-yl)benzene
  • 1-(4-Fluorophenyl)pyrrolidin-2-one 97%
CAS:
54660-08-1
MF:
C10H10FNO
MW:
179.19
Product Categories:
  • Halides
  • Phenyls & Phenyl-Het
Mol File:
54660-08-1.mol
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1-(4-FLUOROPHENYL)-2-PYRROLIDINONE Chemical Properties

Melting point:
55-58 °C
Density 
1.1545 (estimate)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
Safety Statements 
24/25
Hazard Note 
Irritant
HS Code 
29339980

MSDS

  • Language:English Provider:ACROS
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1-(4-FLUOROPHENYL)-2-PYRROLIDINONE Usage And Synthesis

Chemical Properties

beige crystalline powder

Synthesis

616-45-5

352-34-1

54660-08-1

General procedure for the synthesis of 1-(4-fluorophenyl)-2-pyrrolidinone from 2-pyrrolidinone and p-fluoroiodobenzene: N-nucleophilic reagent (2.21 mmol), Cu2O (Sigma-Aldrich, 99.99% purity, 0.147-0.294 mmol), K3PO4 (2.94 mmol), aryl halide (1.47 mmol), phase transfer catalyst (0.147-0.294 mmol) and water (0.40 mL) were sequentially added to the reaction vial and sealed by installing a screw cap. The reaction mixture was stirred in a closed system at 130 °C for 24 h under air atmosphere. Upon completion of the reaction, the non-homogeneous mixture was cooled to room temperature and diluted with dichloromethane. The resulting solution was filtered directly through diatomaceous earth. The organic extracts were combined, dried with anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography to afford the N-arylated product 1-(4-fluorophenyl)-2-pyrrolidinone. The structure and purity of the product were confirmed by 1H NMR and 13C NMR spectral analysis.

References

[1] Tetrahedron Letters, 2011, vol. 52, # 11, p. 1169 - 1172
[2] Synlett, 2015, vol. 26, # 12, p. 1697 - 1701
[3] Advanced Synthesis and Catalysis, 2018, vol. 360, # 11, p. 2178 - 2182

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