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193480-28-3

193480-28-3 Structure

193480-28-3 Structure
IdentificationMore
[Name]

1-BOC-2-BENZYL-PIPERIDIN-4-ONE
[CAS]

193480-28-3
[Synonyms]

1-BOC-2-BENZYL-PIPERIDIN-4-ONE
1-N-BOC-2-BENZYL-PIPERIDIN-4-ONE
1-Boc-2-Benzyl-4-piperidinone
[EINECS(EC#)]

200-589-5
[Molecular Formula]

C17H23NO3
[MDL Number]

MFCD04035610
[Molecular Weight]

289.37
[MOL File]

193480-28-3.mol
Chemical PropertiesBack Directory
[Melting point ]

79-80o C
[Boiling point ]

409.0±38.0 °C(Predicted)
[density ]

1.115±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

-1.58±0.40(Predicted)
[color ]

White to Off-White
[CAS DataBase Reference]

193480-28-3(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-51
Spectrum DetailBack Directory
[Spectrum Detail]

1-BOC-2-BENZYL-PIPERIDIN-4-ONE(193480-28-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-BENZYL-PIPERIDIN-4-ONE

193469-44-2

Carbonic acid, bis(1,1-dimethylethyl) ester

34619-03-9

1-BOC-2-BENZYL-PIPERIDIN-4-ONE

193480-28-3

2-Benzylpiperidin-4-one (17 g) and di-tert-butyl carbonate (21.8 g) were mixed in dichloromethane (500 ml). The reaction mixture was stirred at room temperature for 48 hours. After completion of the reaction, the solvent was removed by rotary evaporation. The organic layer was separated by dissolving the residue in water and toluene. The aqueous layer was extracted again with toluene. All organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated to give 38 g (100% yield) of (±)-1-tert-butoxycarbonyl-2-benzyl-4-piperidone (Intermediate 6).

[References]

[1] Patent: US6346540, 2002, B1. Location in patent: Page column 17
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