## Abstract The syntheses of monofluorinated amino‐alcohols (with primary, secondary and tertiary amino groups and also with quaternary ammonium groups) and of their phosphoric and acetic esters are described.
Recherches sur la formation et la transformation de dérivés organiques du fluor IV. Sur la phosphorylation d'alcools fluorés par l'acide polyphosphorique et sur la vitesse de scission du fluor et de la liaison ester phosphorique des esters fluoralcoylphosphoriques obtenus
✍ Scribed by Emile Cherbuliez; Br. Baehler; G. Cordahi; F. Hunkeler; H. Probst; A. de Picciotto; A. R. Sussmann; A. Yazgi; J. Rabinowitz
- Publisher
- John Wiley and Sons
- Year
- 1960
- Tongue
- German
- Weight
- 524 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Some new fluorinated phosphoric esters are described. The rate of hydrolysis of the organic fluorine and of the phosphoric ester bond is studied. The phosphoric ester group has a stabilizing effect on the fluorine in alkaline medium, whereas the fluorine has a labilizing effect on the phosphoric ester group in acid medium (pH 4,5 and HCl 1N). In all the derivatives where only one atom of fluorine is fixed on one atom of carbon, the fluorine is very easily hydrolysed in alkaline medium. When 2 atoms of F are fixed on the same atom of C, the fluorine derivative is stable in alkaline medium.
📜 SIMILAR VOLUMES
## Abstract Hydroxy nitriles when treated with polyphosphoric acid yield the corresponding carbamido‐alkyl phosphoric acids; but when treated with POCl~3~ in the presence of a tertiary base they yield the corresponding cyano‐alkyl phosphoric acids. β‐cyanoethyl phosphoric acid is very easily dephos
3,3‐dimethylpentane‐2,4‐diol, a new diol, and its dicarbamate have been prepared. Some N,N‐diethylcarbamates of diols have also been prepared from N,N‐diethylcarbamoyl chloride and the corresponding diols.
Some new diethylcarbamates of dialkylamino‐alcohols of type I (fluorinated or not) have been prepared from diethylcarbamylchloride and the corresponding aminoalcohols.
## Abstract Some new fluorinated hydroxy‐acids and hydroxy‐ethers as well as their phosphorylated derivatives are described.
Phosphorous acid does not dehydrate tertiary alcohols at temperatures below 100 "C ; but the esterification reaction is very slow and phosphorous monoesters of tertiary alcohols cannot be obtained this way. Although this reaction is also slow with phenol, phenyl phosphorous monoester can be obtained