130288-82-3

Basic information

• Product Name: C₁₅H₂₇O₆P
• Synonyms: C₁₅H₂₇O₆P
• CAS NO: 130288-82-3
• Molecular Weight: 334.35
• Mol File: 130288-82-3.mol

Chemical Properties

• CAS DataBase Reference: C₁₅H₂₇O₆P(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₂₇O₆P(130288-82-3)
• EPA Substance Registry System: C₁₅H₂₇O₆P(130288-82-3)

Safety Data

• Hazardous Substances Data: 130288-82-3(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 54921-72-1 phenyl H-phosphonate ammonium salt 
• 183544-77-6 phenyl H-phosphonate 

Downstream Products

• 48014-95-5 ethyl H-phosphonate 
• 762-04-9 phosphonic acid diethyl ester 
• 122-52-1 triethyl phosphite 

Relevant articles and documents

Studies on aryl H-phosphonates. 3. Mechanistic investigations related to the disproportionation of diphenyl H-phosphonate under anhydrous basic conditions

Diphenyl H-phosphonate undergoes under anhydrous reaction conditions a base-promoted disproportionation to triphenyl phosphite and phenyl H- phosphonate. On the basis of 31P NMR data the most likely mechanism for this transformation was proposed. In order to substantiate these findings and to get a deeper insight into the chemistry of aryl H-phosphonate esters, we carried out also some studies on activation of phenyl and diphenyl H- phosphonates with various condensing agents. We found that aryl vs alkyl esters of phosphonic acid often follow different reaction pathways during the activation, and this can most likely be traced back to higher electrophilicity of the phosphorus centre and to higher reactivity of the P- H bonds in aryl H-phosphonate derivatives.

31P NMR Studies on the Activation Pathways of Aryl H-Phosphonate esters with Condensing Agents

Diaryl and akyl aryl H-phosphonate diesters, in contradiction to the dialkyl derivatives, undergo in the presence of condensing agents (pivaloyl chloride, chlorophosphates, 2,4,6-triisopropylbenzenesulfonyl chloride, dicyclohexylcarbodiimide) activation producing reactive tervalent P(III) intermediates.Phenyl H-phosphonate reacts similarly to the alkyl esters affording acyl derivatives (with pivaloyl chloride) or triphenyl trimetaphosphite (with the other coupling agents).In the latter instance, depending on the reaction conditions, species with C3v or Cs symmetry are formed.