4-Piperidinone, 1-(4-nitrophenyl)-
- Product Name
- 4-Piperidinone, 1-(4-nitrophenyl)-
- CAS No.
- 23499-01-6
- Chemical Name
- 4-Piperidinone, 1-(4-nitrophenyl)-
- Synonyms
- 1-(4-nitrophenyl)-4-piperidinone;1-(4-NITROPHENYL)PIPERIDINE-4-ONE;4-Piperidinone, 1-(4-nitrophenyl)-;2(3H)-Benzoxazolone,6-bromo-6-(triphenylmethyl)-
- CBNumber
- CB22639338
- Molecular Formula
- C11H12N2O3
- Formula Weight
- 220.22
- MOL File
- 23499-01-6.mol
4-Piperidinone, 1-(4-nitrophenyl)- Property
- Melting point:
- 167.0-167.5 °C
- Boiling point:
- 422.7±40.0 °C(Predicted)
- Density
- 1.295±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 0.81±0.40(Predicted)
- Appearance
- Light yellow to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- N926558
- Product name
- 1-(4-Nitrophenyl)piperidin-4-one
- Packaging
- 50mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- CHM0126815
- Product name
- 1-(4-NITROPHENYL)TETRAHYDRO-4(1H)-PYRIDINONE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $808.89
- Updated
- 2021/12/16
- Product number
- CHM0126815
- Product name
- 1-(4-NITROPHENYL)TETRAHYDRO-4(1H)-PYRIDINONE
- Purity
- 95.00%
- Packaging
- 2.5G
- Price
- $1147.43
- Updated
- 2021/12/16
- Product number
- CHM0126815
- Product name
- 1-(4-NITROPHENYL)TETRAHYDRO-4(1H)-PYRIDINONE
- Purity
- 95.00%
- Packaging
- 5G
- Price
- $1421.65
- Updated
- 2021/12/16
- Product number
- 1444AL
- Product name
- 1-(4-Nitrophenyl)piperidin-4-one
- Packaging
- 1g
- Price
- $143
- Updated
- 2021/12/16
4-Piperidinone, 1-(4-nitrophenyl)- Chemical Properties,Usage,Production
Synthesis
350-46-9
23499-01-6
General procedure for the synthesis of 1-(4-nitrophenyl)-piperidin-4-one from p-fluoronitrobenzene: To acetonitrile (20 mL) were added 4-piperidinone hydrochloride (2.17 g, 16.0 mmol), triethylamine (3.9 mL), and potassium carbonate (2.9 g, 21.0 mmol) sequentially. After stirring for 20 minutes at room temperature, 1-fluoro-4-nitrobenzene (1 g, 7.09 mmol) was added and the reaction mixture was heated to reflux for 12 hours. After completion of the reaction, it was cooled to room temperature, filtered and the filtrate was concentrated under reduced pressure to obtain the crude product. The crude product was dissolved in water and extracted with ethyl acetate, the organic phase was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give 1-(4-nitrophenyl)-piperidin-4-one (0.6 g, 38% yield).
References
[1] Patent: WO2006/123145, 2006, A1. Location in patent: Page/Page column 54-55
[2] Synthesis, 1981, # 8, p. 606 - 608
[3] Synthesis, 1981, # 8, p. 606 - 608
[4] European Journal of Medicinal Chemistry, 2013, vol. 66, p. 32 - 45
[5] Patent: CN106905245, 2017, A
4-Piperidinone, 1-(4-nitrophenyl)- Preparation Products And Raw materials
Raw materials
Preparation Products
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