| 1-(Benzyloxycarbonyl)-4-piperidinone Usage And Synthesis |
| 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.3 |
| General Description |
1-Z-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions.
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| 1-(Benzyloxycarbonyl)-4-piperidinone Preparation Products And Raw materials |
| Raw materials | 1-[(Benzyloxy)carbonyl]piperidine-4-carboxylic acid-->8-(BENZYLOXYCARBONYL)-1,4-DIOXA-8-AZASPIRO[4.5]DECANE-->cyclohexylmethyl chloroformate-->1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-4-[[(trifluoroMethyl)sulfonyl]oxy]-, phenylMethyl ester-->N-(Benzyloxycarbonyloxy)succinimide-->Benzyl chloroformate-->Benzyl 4-hydroxy-1-piperidinecarboxylate-->4-Hydroxypiperidine |
| Preparation Products | 2-Piperidone-->Ethyl 1-Cbz-5-oxoazepane-4-carboxylate |