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17677-92-8

17677-92-8 Structure

17677-92-8 Structure
IdentificationBack Directory
[Name]

BIS(2,2,2-TRICHLORO-1,1-DIMETHYLETHYL) PHOSPHOROCHLORIDATE
[CAS]

17677-92-8
[Synonyms]

BIS(2,2,2-TRICHLORO-1,1-DIMETHYLETHYL) PHOSPHOROCHLORIDATE
[Molecular Formula]

C8H12Cl7O3P
[MOL File]

17677-92-8.mol
[Molecular Weight]

435.324
Chemical PropertiesBack Directory
[Melting point ]

mp 81-82 °C
[solubility ]

crystallized from pentane
[form ]

colorless solid
Hazard InformationBack Directory
[Uses]

BIS(2,2,2-TRICHLORO-1,1-DIMETHYLETHYL) PHOSPHOROCHLORIDATE is used as a phosphorylating reagent.
[Synthesis]

Bis(2,2,2-trichloro-1,1-dimethylethyl) Phosphorochloridate is conveniently prepared by the reaction of 2-trichloromethyl-2-propanol with PCl3 in pyridine solvent to afford bis(2,2,2-trichloro-1,1-dimethylethyl) chlorophosphite (71%). The chlorophosphite is oxidized with (Diacetoxyiodo)benzene to give 65% of the desired phosphorochloridate (eq 1). This overall procedure represents an improved synthesis of the phosphorochloridate when compared to the different methods reported in the literature, which give mixtures of bis(2,2,2-trichloro-1,1-dimethylethyl) chlorophosphite and 2,2,2-trichloro-1,1-dimethylethyl dichlorophosphite.[1][2]BIS(2,2,2-TRICHLORO-1,1-DIMETHYLETHYL) PHOSPHOROCHLORIDATE synthesis method
[Synthesis Reference(s)]

[1](a) Gerrard, W. JCS 1944, 85. (b) Gerrard, W.; Wyvill, P. L. Research (London) 1949, 2, 536. (c) Gerrard, W.; Isaacs, M. J. D.; Machell, G.; Smith, K. B.; Wyvill, P. L. JCS 1953, 1920. (d) Gerrard, W.; Green, W. J.; Phillips, R. J. JCS 1954, 1148.
[2] (a) Abramov, V. S.; Khairullin, V. K. JGU 1957, 27, 501. (b) Sasse, K. MOC 1964, XII/2, 45.
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