Basic information Safety Supplier Related

1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE

Basic information Safety Supplier Related

1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE Basic information

Product Name:
1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE
Synonyms:
  • 1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE
  • 1-Benzylazepan-4-one
  • 1-Benzylhexahydro-4-azepinone
  • 4H-Azepin-4-one,hexahydro-1-(phenylmethyl)-
  • N-Benzylazepane-4-one
  • 4H-Azepin-4-one
  • hexahydro-1-(phenylMethyl)-
  • 1-benzyl-4-azepanone
CAS:
1208-75-9
MF:
C13H17NO
MW:
203.28
Product Categories:
  • pharmacetical
Mol File:
1208-75-9.mol
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1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE Chemical Properties

Boiling point:
115-118 °C(Press: 0.01 Torr)
Density 
1.069
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
7.61±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
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1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE Usage And Synthesis

Synthesis

50492-22-3

100-39-0

1208-75-9

Potassium carbonate (K2CO3, 12 g, 88 mmol, 3.0 eq.) was added to acetone (10 mL) as 4-azepinone hydrochloride (1-18, 4.4 g, 29 mmol) and benzyl bromide (5.0 g, 29 mmol, 1.0 eq.). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the crude reaction mixture was concentrated by evaporation, the residue was dissolved in ethyl acetate and the organic layer was washed with water. The crude product was purified by silica gel column chromatography to afford 1-benzylhexahydroazepin-4-one (1-19, 5.6 g, 95% yield). Mass spectrometric (ESI) analysis showed m/z 204.1 (M + H+).

References

[1] Patent: WO2010/144571, 2010, A1. Location in patent: Page/Page column 133-134
[2] Patent: WO2015/140559, 2015, A1. Location in patent: Page/Page column 50; 51
[3] Patent: US2013/143870, 2013, A1. Location in patent: Paragraph 0489; 0490
[4] Patent: US2013/150341, 2013, A1. Location in patent: Paragraph 0418; 0419
[5] Patent: WO2013/83741, 2013, A1. Location in patent: Page/Page column 98

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