98014-60-9

Basic information

• Product Name: tert-butyl N-benzyl-N-(1-methyl-3-oxopropyl)carbamate
• Synonyms: tert-butyl N-benzyl-N-(1-methyl-3-oxopropyl)carbamate
• CAS NO: 98014-60-9
• Molecular Weight: 277.364
• Mol File: 98014-60-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl N-benzyl-N-(1-methyl-3-oxopropyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl N-benzyl-N-(1-methyl-3-oxopropyl)carbamate(98014-60-9)
• EPA Substance Registry System: tert-butyl N-benzyl-N-(1-methyl-3-oxopropyl)carbamate(98014-60-9)

Safety Data

• Hazardous Substances Data: 98014-60-9(Hazardous Substances Data)

Upstream product

• 98014-59-6 Benzyl-(3-hydroxy-1-methyl-propyl)-carbamic acid tert-butyl ester 
• 507444-65-7 methyl 3-(benzylamino)butanoate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 6335-80-4 ethyl 3-(benzylamino)butanoate 

Downstream Products

• 98014-61-0 Benzyl-((3Z,5E)-1-methyl-hepta-3,5-dienyl)-carbamic acid tert-butyl ester 
• 98014-62-1 Benzyl-((3E,5E)-1-methyl-hepta-3,5-dienyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Stereoselective Synthesis of Piperidines by Iridium-Catalyzed Cyclocondensation

An iridium-catalyzed cyclocondensation of amino alcohols and aldehydes is reported. Intramolecular allylic substitution by an enamine intermediate and subsequent in situ reduction furnishes 3,4-disubstituted piperidines with high enantiospecificity and good diastereoselectivity. The modular approach and the broad functional group tolerance provide access to diverse piperidine derivatives, which were further functionalized to give a versatile set of products.