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ChemicalBook--->CAS DataBase List--->28566-14-5

28566-14-5

28566-14-5 Structure

28566-14-5 Structure
IdentificationBack Directory
[Name]

6,7-DIHYDRO-5H-1-PYRIDIN-5-ONE
[CAS]

28566-14-5
[Synonyms]

112208
6,7-DIHYDRO-5H-1-PYRIDIN-5-ONE
6,7-DIHYDRO-5H-[1]PYRINDIN-5-ONE
6H,7H-cyclopenta[b]pyridin-5-one
5H,6H,7H-cyclopenta[b]pyridin-5-one
6,7-dihydrocyclopenta[b]pyridin-5-one
6,7-DIHYDRO-5H-CYCLOPENTA[B]PYRIDIN-5-ONE
6,7-Dihydro-5-oxo-5H-cyclopenta[b]pyridine
5H-cyclopenta[b]pyridine-5-one,6,7-dihydro-
5H-Cyclopenta[b]pyridin-5-one, 6,7-dihydro-
6,7-DIHYDRO-5H-1-PYRIDIN-5-ONE ISO 9001:2015 REACH
[Molecular Formula]

C8H7NO
[MDL Number]

MFCD07371500
[MOL File]

28566-14-5.mol
[Molecular Weight]

133.15
Chemical PropertiesBack Directory
[Melting point ]

64-66 °C
[Boiling point ]

125 °C(Press: 9 Torr)
[density ]

1.230±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

3.47±0.20(Predicted)
[Appearance]

Gray to brown Solid
[InChI]

InChI=1S/C8H7NO/c10-8-4-3-7-6(8)2-1-5-9-7/h1-2,5H,3-4H2
[InChIKey]

LMEREVKJVWUGJI-UHFFFAOYSA-N
[SMILES]

C12CCC(=O)C1=CC=CN=2
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H317-H319
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

6,7-DIHYDRO-5H-1-PYRIDIN-5-ONE(28566-14-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Cyclopenta[b]pyridine

533-37-9

6,7-DIHYDRO-5H-1-PYRIDIN-5-ONE

28566-14-5

The general procedure for the synthesis of 6,7-dihydrocyclopenta[b]pyridin-5-one using 2,3-cyclopentenopyridine as starting material was as follows: 0.883 mg of Mn(OTf)2 (0.5 mol%), 60 mg of 2,3-cyclopentenopyridine, 0.35 g of 65% aqueous TBHP and 2.5 mL of water were added sequentially to 25 mL of a round bottomed flask. The reaction system was stirred in air at room temperature for 24 hours. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate (3 × 5 mL), the organic phases were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was removed by distillation under reduced pressure. The crude product was purified by silica gel column chromatography using petroleum ether and ethyl acetate (5:1, v/v) as eluent to afford 60.5 mg of 6,7-dihydro-5H-cyclopentadieno[b]pyridin-5-one as a light yellow solid in 91% yield.

[References]

[1] Patent: CN105669548, 2016, A. Location in patent: Paragraph 0027; 0028
[2] Angewandte Chemie - International Edition, 2018, vol. 57, # 15, p. 4078 - 4082
[3] Angew. Chem., 2018, vol. 130, # 15, p. 4142 - 4146,5
[4] Chinese Journal of Catalysis, 2016, vol. 37, # 8, p. 1216 - 1221
[5] Organic Letters, 2018, vol. 20, # 7, p. 1987 - 1990
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533-37-9

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