THE FORMATION OF α-AMINO AND α-HYDROXY-ALKANEPHOSPHONIC ACIDS IN THE REACTIONS OF PHOSPHITE ESTERS WITH ALDEHYDES AND ALKYL CARBAMATES

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• In certain experiments (Tables I and II) a 50% excess of aldehyde was used in order to compensate for probable loss of this volatile reactant from the reaction system under reflux. The results using equimolar quantities of all reagents are given in Table III and show the presence in the final product of unreacted phosphite (δp 127.7) and also a second P(III) derivative (δp 129.9), which may possibly be an acetyl phosphite. Small amounts of the oxidation products triphenyl phosphate (δp -18.0) and diphenyl phosphate (δp-10.0) were also detected.
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