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2‐Hydroperfluoropropyl azide—a versatile reagent for the oxidative fluorination of organic compounds of trivalent phosphorus

2‐Hydroperfluoropropyl azide—a versatile reagent for the oxidative fluorination of organic... 2‐Hydroperfluoropropyl azide CF3CHFCF2N3, 1, an inexpensive, readily available, and stable (easy to store) compound, is suggested as an effective fluorinating reagent for different classes of trivalent organophosphorus compounds in accordance with the general scheme R3P → R3PF2. Generally, the reactions are performed without solvent, the highly volatile CF3 CHFCN being the main by‐product. The fluorination is usually an exothermic process, but slight heating is necessary in the case of alkyldifluorophosphites. The unusual Arbuzov rearrangement, accompanied by isomerization of an isobutyl or neopentyl group into a tert‐group, ROPF2 → t‐R′POF2, under the action of a catalytic amount of 1, was observed. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

2‐Hydroperfluoropropyl azide—a versatile reagent for the oxidative fluorination of organic compounds of trivalent phosphorus

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References (9)

Publisher
Wiley
Copyright
Copyright © 1993 Wiley Subscription Services
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.520040610
Publisher site
See Article on Publisher Site

Abstract

2‐Hydroperfluoropropyl azide CF3CHFCF2N3, 1, an inexpensive, readily available, and stable (easy to store) compound, is suggested as an effective fluorinating reagent for different classes of trivalent organophosphorus compounds in accordance with the general scheme R3P → R3PF2. Generally, the reactions are performed without solvent, the highly volatile CF3 CHFCN being the main by‐product. The fluorination is usually an exothermic process, but slight heating is necessary in the case of alkyldifluorophosphites. The unusual Arbuzov rearrangement, accompanied by isomerization of an isobutyl or neopentyl group into a tert‐group, ROPF2 → t‐R′POF2, under the action of a catalytic amount of 1, was observed.

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 1993

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