1-(Benzyloxycarbonyl)-4-piperidinone CAS 19099-93-5

“N-Benzyloxycarbonyl-4-piperidone
1-benzyloxycarbonyl-piperidin-4-one
1-carbobenzyloxy-4-piperidone
1-Cbz-4-piperidinone
Benzyl 4-oxo-1-piperidinecarboxylate
1-Piperidinecarboxylic acid, 4-oxo-, phenylmethyl ester
1-(Benzyloxycarbonyl)-4-piperidinone
1-Z-4-Piperidone
4-Oxo-1-piperidinecarboxylic Acid Benzyl Ester
1-Cbz-4-piperidone
benzyl 4-oxopiperidine-1-carboxylate
1-Cbz-piperidin-4-one
1-Benzyloxycarbonyl-4-piperidine
N-CBZ-4-piperidone
1-Carbobenzoxy-4-piperidone
4-oxo-piperidine-1-carboxylic acid benzyl ester
MFCD00673144”

“Chemical Properties
Colourless Oil

Uses
Protected piperidinone that can undergo interesting synthetic transformations including the Knoevenagel reaction,1 hetero-Diels-Alder reactions,2 and reactions to form N-(4-piperidinyl)oxindoles.

General Description
1-Z-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions.
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Protective piperidone can be used for synthesis and transformation reactions that have attracted much attention, including Knoevenagel reaction, heterogeneous Diels-Alder reaction, and the formation of N-(4-piperidyl) hydroxyindole. The raw material for synthesis of GABA analogues by direct Barbier- type addition reaction of alkyl phosphonate.

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