ChemicalBook--->CAS DataBase List--->173186-91-9

173186-91-9

173186-91-9 Structure

173186-91-9 Structure
IdentificationBack Directory
[Name]

1-BENZYL-3,3-DIMETHYL-PIPERIDIN-4-ONE
[CAS]

173186-91-9
[Synonyms]

1-Benzyl-3,3-dimethyl-4-piperidone
N-Benzyl-3,3-dimethyl-4-piperidone
1-BENZYL-3,3-DIMETHYL-PIPERIDIN-4-ONE
3,3-dimethyl-1-(phenylmethyl)-4-piperidinone
4-Piperidinone, 3,3-dimethyl-1-(phenylmethyl)-
1-BENZYL-3,3-DIMETHYL-PIPERIDIN-4-ONE ISO 9001:2015 REACH
[Molecular Formula]

C14H19NO
[MDL Number]

MFCD09908040
[MOL File]

173186-91-9.mol
[Molecular Weight]

217.31
Chemical PropertiesBack Directory
[Boiling point ]

318.0±22.0 °C(Predicted)
[density ]

1.031±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

7.14±0.40(Predicted)
[Appearance]

White to yellow Solid-Liquid Mixture
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

1-BENZYL-3,3-DIMETHYL-PIPERIDIN-4-ONE(173186-91-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-PIPERIDINOL, 3,3-DIMETHYL-1-(PHENYLMETHYL)-

324769-02-0

1-BENZYL-3,3-DIMETHYL-PIPERIDIN-4-ONE

173186-91-9

Oxidation Procedure: 0.40 mL (5.6 mmol) of dimethyl sulfoxide was dissolved in 5 mL of dichloromethane and cooled to -78 °C. 0.35 mL (2.48 mmol) of trifluoroacetic anhydride was slowly added dropwise under stirring and stirring was continued for 30 minutes. Subsequently, 0.25 g (1.14 mmol) of a 2 mL solution of 1-benzyl-3,3-dimethyl-4-hydroxypiperidine in dichloromethane was added dropwise, and the reaction mixture was stirred at -78 °C for 1 hour. Then, 1.0 mL (7.2 mmol) of triethylamine was added and the reaction mixture was slowly warmed to 0°C and stirred at this temperature for 2 hours. After completion of the reaction, the mixture was poured into water and extracted with ethyl acetate. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent being a hexane solution of 0-20% ethyl acetate. The fraction containing the target product was collected and concentrated under reduced pressure to give 0.20 g (79% yield) of 3,3-dimethyl-1-phenylmethyl-piperidin-4-one.

[References]

[1] Patent: EP1204659, 2003, B1. Location in patent: Page/Page column 26
[2] Patent: EP1204660, 2004, B1. Location in patent: Page 15
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