175913-71-0

Basic information

• Product Name: (4S,5S)-4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-methyl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-heptanoic acid ethyl ester
• CAS NO: 175913-71-0
• Molecular Weight: 591.643
• Mol File: 175913-71-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5S)-4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-methyl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-heptanoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-methyl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-heptanoic acid ethyl ester(175913-71-0)
• EPA Substance Registry System: (4S,5S)-4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-5-methyl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-heptanoic acid ethyl ester(175913-71-0)

Safety Data

• Hazardous Substances Data: 175913-71-0(Hazardous Substances Data)

Upstream product

• 22509-74-6 N-ethoxycarbonylphthalimide 
• 73-32-5 L-isoleucine 
• 29588-88-3 N-phthaloyl-L-isoleucine 
• 126926-31-6 (2S,3S)-2-(1,3-dioxoisoindolin-2-yl)-3-methylpentanoyl chloride 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Relevant articles and documents

Flash vacuum pyrolysis of stabilised phosphorus ylides. Part 7. Cyclisation of amino acid derived α-phthalimidoacyl ylides to give pyrroloisoindolediones

A series of 11 amino acid-derived stabilised ylides 12-14 and 16 have been prepared and characterised. In one case, for compound 17, an X-ray structure determination supports formulation of the compounds as phosphonium enolates. Flash vacuum pyrolysis (FVP) of 12 and 13 at 500°C results in loss of R23PO between the ylide function and one carbonyl of the phthalimido group to give products characterised spectroscopically as the pyrroloisoindolediones 18. The identity of these is also supported by the results of 13C and 15N labelling experiments, but owing to their high reactivity complete separation from the phosphine oxide was not generally possible even when Bu3PO rather than Ph3PO was involved. Chromatographic purification of 29, similarly produced by FVP of 14, led to partial hydrolysis, rearrangement and decarboxylation to give 30. FVP of 12 at 750°C gave the 1-unsubstituted pyrroloisoindolediones 19 in two cases.