ChemicalBook--->CAS DataBase List--->175406-94-7

175406-94-7

175406-94-7 Structure

175406-94-7 Structure
IdentificationBack Directory
[Name]

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride
[CAS]

175406-94-7
[Synonyms]

Methyl 1-benzyl-3-oxopiperidine-4-carboxylate
Methyl 1-benzyl-3-oxo-4-piperidinecarboxylate
ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride
4-Piperidinecarboxylic acid, 3-oxo-1-(phenylmethyl)-, methyl ester
[Molecular Formula]

C14H17NO3
[MDL Number]

MFCD00012792
[MOL File]

175406-94-7.mol
[Molecular Weight]

247.29
Chemical PropertiesBack Directory
[Boiling point ]

354.4±42.0 °C(Predicted)
[density ]

1.177±0.06 g/cm3(Predicted)
[pka]

10.83±0.20(Predicted)
Hazard InformationBack Directory
[Synthesis]

1-Benzyl-3-piperidone

40114-49-6

Dimethyl carbonate

616-38-6

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride

175406-94-7

To a stirred mixture of 1-benzyl-3-piperidone (72 g) and dimethyl carbonate (500 mL) was added sodium hydride (38 g, 60% oil dispersion) in batches. The reaction mixture was heated to reflux for 20 min and then the reaction was quenched by the slow addition of water (800 mL). The aqueous phase was extracted with ethyl acetate (3 x 400 mL), the organic phases were combined and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure to give methyl 1-benzyl-3-oxopiperidine-4-carboxylate as a brown oil (93 g, 99% yield). lc-MS (ESI+): m/z 248 [M+H]+.

[References]

[1] Patent: WO2009/26241, 2009, A1. Location in patent: Page/Page column 77-78
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40114-49-6

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