84494-64-4

Basic information

• Product Name: 3-methyl-r-2,c-4,c-5-triphenyloxazolidine
• CAS NO: 84494-64-4
• Molecular Weight: 315.415
• Mol File: 84494-64-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-methyl-r-2,c-4,c-5-triphenyloxazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-r-2,c-4,c-5-triphenyloxazolidine(84494-64-4)
• EPA Substance Registry System: 3-methyl-r-2,c-4,c-5-triphenyloxazolidine(84494-64-4)

Safety Data

• Hazardous Substances Data: 84494-64-4(Hazardous Substances Data)

Upstream product

• 550-58-3 N-methylamino-2 diphenyl-1,2 ethanol erythro 
• 100-52-7 benzaldehyde 
• 908094-04-2 phenyldiazomethane 
• 71653-79-7 cis-1-methyl-2,3-diphenylaziridine 
• 84494-64-4 3-methyl-r-2,t-4,c-5-triphenyloxazolidine 
• 550-58-3 DL-threo-2-methylamino-1.2-diphenyl-ethanol 
• 107-97-1 sarcosine 
• 622-29-7 N-Benzylidenemethylamine 
• 103-67-3 benzyl-methyl-amine 

Downstream Products

• 84494-64-4 3-methyl-r-2,c-4,t-5-triphenyloxazolidine 

Relevant articles and documents

Synthesis of 2,4,5-triphenyl-substituted oxazolidine and 2,5-diphenyl-substituted pyrrolidine derivatives

A simple one-pot domino reaction procedure for the stereoselective synthesis of oxazolidines and C2-symmetric pyrrolidines from inexpensive starting materials is described. Azomethine ylides generated in situ by heating a mixture of benzaldehyde and benzylic amines are trapped with dipolarophiles by a 1,3-dipolar cycloaddition reaction. The products represent valuable synthetic building blocks or potential starting materials for the preparation of chiral auxiliaries and are difficult to obtain by other methods.

AZIRIDINES-IV CATALYTIC DECOMPOSITION OF PHENYLDIAZOMETHANE IN SCHIFF'S BASES

Catalytic decomposition of phenyldiazomethane in Schiff's bases is found to proceed via formation of trans-1,3-dipole (azomethine ylide) as an intermediate product.Depending on the size and quantity of the substituents, the ylide undergoes either cyclizat