Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Diethyl phosphite is the organophosphorus compound with the formula (C2H5O)2P(O)H. It is a popular reagent for generating other organophosphorus compounds, exploiting the high reactivity of the P-H bond. Diethyl phosphite is a colorless liquid.[1] The molecule is tetrahedral.
^Green, Kenneth (2001). "Diethyl Phosphonite". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rd211. ISBN 0471936235.
by heating diethylphosphite in methanol. Although studies have not been reported for this compound, the closely related diethylphosphite exists predominantly...
non-uniform electric field Diethyl phthalate, an organic compound Diethylphosphite, an organophosphorus compound Dépanneur, Quebec English term for a...
the base, the reaction of ethanol and phosphorus trichloride affords diethylphosphite ((EtO)2P(O)H). Of the many related compounds can be prepared similarly...
molecule is tetrahedral. The compound is prepared by the chlorination of diethylphosphite with carbon tetrachloride (Atherton–Todd reaction). The compound is...
oxide can be prepared by the reaction of phosphonic esters, such as diethylphosphite, with Grignard reagents followed by acid workup: (C2H5O)2P(O)H + 3 C6H5MgBr...
generic imine, RCH=NR', would react with a phosphorous reagent like diethylphosphite as follows: RCH=NR' + (EtO)2P(O)H → (EtO)2P(O)CHR-NHR' In addition...
dimethylphosphine oxide have been developed. A popular method starts with diethylphosphite, according to the following idealized equations: (C2H5O)2P(O)H + 3...
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