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Chemical Structure| 1072-83-9 Chemical Structure| 1072-83-9
Chemical Structure| 1072-83-9

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CAS No.: 1072-83-9

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Product Details of 2-Acetylpyrrole

CAS No. :1072-83-9
Formula : C6H7NO
M.W : 109.13
SMILES Code : CC(=O)C1=CC=CN1
MDL No. :MFCD00005220
InChI Key :IGJQUJNPMOYEJY-UHFFFAOYSA-N
Pubchem ID :14079

Safety of 2-Acetylpyrrole

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2-Acetylpyrrole

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1072-83-9 ]

[ 1072-83-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1072-83-9 ]
  • [ 14150-94-8 ]
  • [ 1203570-45-9 ]
  • 2
  • chitosan, Mw = 760000, degree of deacetylation DD = 85.5%, [ No CAS ]
  • [ 109-08-0 ]
  • [ 1122-62-9 ]
  • [ 1192-62-7 ]
  • [ 2214-53-1 ]
  • [ 85279-30-7 ]
  • [ 1072-83-9 ]
  • [ 1262900-24-2 ]
  • [ 99969-04-7 ]
  • [ 32736-95-1 ]
  • [ 74376-36-6 ]
  • 3
  • [ 1072-83-9 ]
  • [ 133730-34-4 ]
  • C14H15NO3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With nickel(II) oxide; potassium carbonate; In ethanol; water; at 50℃; for 24h; General procedure: The general procedure for C-N coupling involves stirringthe mixture of phenyl boronic acid (1mmol), nucleophileslike pyrrole or indole (1.5mmol) and NiO catalyst (7mg)in 5ml of solvent at 50C. The progress of the reactionwas monitored by thin layer chromatography (TLC) using petroleum ether and ethyl acetate as eluting solvents. Afterthe completion of reaction, the reaction mixture was mixedwith 15ml distilled water and 15ml ethyl acetate to separatethe aqueous and organic layers. The resulting organic layerswere collected together, washed and dried. The raw productwas separated by preparative thin layer chromatographyusing the same eluents petroleum ether and ethyl acetate.The formation of N-arylated products were confirmed byNMR and GC-MS analysis.
 

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