ChemicalBook--->CAS DataBase List--->160357-94-8

160357-94-8

160357-94-8 Structure

160357-94-8 Structure
IdentificationMore
[Name]

1-Acetylpiperidin-4-amine
[CAS]

160357-94-8
[Synonyms]

1-(4-AMINO-PIPERIDIN-1-YL)-ETHANONE
1-ACETYLPIPERIDIN-4-AMINE
4-AMINO-1-ACETYL-PIPERIDINE
4-Amino-N-1-acetylpiperidine
1-ACETYL-4-AMINO-PIPERIDINE
[Molecular Formula]

C7H14N2O
[MDL Number]

MFCD03412449
[Molecular Weight]

142.2
[MOL File]

160357-94-8.mol
Chemical PropertiesBack Directory
[Boiling point ]

273.6±33.0 °C(Predicted)
[density ]

1.042±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

oil
[pka]

9.37±0.20(Predicted)
[color ]

Colourless to light yellow
[InChI]

InChI=1S/C7H14N2O/c1-6(10)9-4-2-7(8)3-5-9/h7H,2-5,8H2,1H3
[InChIKey]

NLHBHVGPMMXWIM-UHFFFAOYSA-N
[SMILES]

C(=O)(N1CCC(N)CC1)C
[CAS DataBase Reference]

160357-94-8(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

1-Acetyl-4-aminopiperidine is a heterocyclic organic compound with a density of 1.042 g/cm3 and a boiling point of 273.6ºCat760 mmHg. It is an important intermediate in the synthesis of piperidine drugs.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22-36
[Safety Statements ]

26
[RIDADR ]

UN2735
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

1-Acetylpiperidin-4-amine(160357-94-8)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

1-Acetylpiperidin-4-amine(160357-94-8)
Hazard InformationBack Directory
[Synthesis]

4-Piperidinone, 1-acetyl-, 4-oxime (9CI)

135581-16-7

1-Acetylpiperidin-4-amine

160357-94-8

General procedure for the synthesis of 4-amino-N-1-acetylpiperidine from 1-acetylpiperidin-4-one (CAS: 135581-16-7, 10 g, 70 mmol): 1. Oximization reaction: 1-acetylpiperidin-4-one was dissolved in 200 mL of ethanol, hydroxylamine hydrochloride (10 g, 143 mmol) and pyridine (10 mL) were added. The reaction mixture was heated to 70 °C and maintained for 1.5 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and the residue was treated with cold water and cooled to 0 °C. The resulting slurry was filtered and dried under vacuum to give 1-acetylpiperidin-4-one oxime (6.5 g, white solid, 59% yield). 2. Hydrogenation reaction: The oxime (2.0 g, 12 mmol) prepared above was dissolved in 50 mL of ethanol, and nickel ruanne (0.2 g) was added after being washed several times with water. The mixture was transferred to a Parr reactor and hydrogenated at 50 psi hydrogen pressure for 16 hours. Upon completion of the reaction, the reaction mixture was carefully filtered and the filtrate was evaporated under reduced pressure to afford 4-amino-N-1-acetylpiperidine (1.7 g, green solid, 100% yield). The product was analyzed by GC-MS, m/z = 142.

[References]

[1] Patent: WO2004/110996, 2004, A1. Location in patent: Page/Page column 102
[2] Patent: US2008/227780, 2008, A1. Location in patent: Page/Page column 55
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