Basic information Safety Supplier Related

2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE

Basic information Safety Supplier Related

2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE Basic information

Product Name:
2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE
Synonyms:
  • 2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE
  • 2,3,4,5-Tetrahydro-1H-2-benzazepin-1-one
  • 2,3,4,5-tetrahydro-1H-2-benzazepine-1-one
  • 1H-2-Benzazepin-1-one, 2,3,4,5-tetrahydro-
  • 2,3,4,5-tetrahydro-2-benzazepin-1-one
  • 2,3,4,5-Tetrahydro-benzo[c]azepin-1-one, CAS 6729-50-6
CAS:
6729-50-6
MF:
C10H11NO
MW:
161.2
Mol File:
6729-50-6.mol
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2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE Chemical Properties

Melting point:
99-100 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
Boiling point:
392.5±12.0 °C(Predicted)
Density 
1.100
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
14.78±0.20(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Hazard Codes 
N
Risk Statements 
51/53
Safety Statements 
61
HS Code 
2933998090
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2,3,4,5-TETRAHYDRO-BENZO[C]AZEPIN-1-ONE Usage And Synthesis

Chemical Properties

White to beige crystalline powder

Synthesis

529-34-0

6729-50-6

General procedure for the synthesis of 2,3,4,5-tetrahydro-1H-2-benzazepin-1-one from 1-tetrahydronaphthalenone: 2.72 g (41.8 mmol) of sodium azide was added batchwise to a solution of concentrated hydrochloric acid (75 mL) containing 6.11 g (41.8 mmol) of 3,4-dihydronaphthalen-1(2H)-one and the reaction was carried out at 0 °C. Subsequently, the reaction was eluted with hydrochloric acid (75 mL) at 0 °C for 1 h. Stirring was continued at 0 °C for 30 min, then slowly warmed to room temperature and the reaction lasted for 16 hours. Upon completion of the reaction, the reaction mixture was poured into ice water and the pH was adjusted with potassium carbonate to 9. The aqueous phase was extracted with dichloromethane (DCM), the organic phases were combined and dried with anhydrous magnesium sulfate (MgSO?), filtered and concentrated under reduced pressure. The residue was purified by recrystallization from hexane. Further purification by column chromatography (silica gel, eluent hexane/ethyl acetate = 1:2) afforded 1.8 g (11.1 mmol, 27% yield) of the target product 2,3,4,5-tetrahydro-1H-2-benzazepin-1-one.

References

[1] Angewandte Chemie - International Edition, 2018, vol. 57, # 38, p. 12347 - 12351
[2] Angew. Chem., 2018, vol. 130, # 38, p. 12527 - 12531,5
[3] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 11, p. 914 - 919
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 13, p. 5287 - 5307
[5] Angewandte Chemie - International Edition, 2017, vol. 56, # 13, p. 3655 - 3659

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