North, Robert Arthur

2019-02-15T14:15:19Z

2019-02-15T14:15:19Z

1979

Reactions of triethyl or trimethyl phosphite with 2- aryl -1-phenyl-1-nitroethenes at elevated temperatures gave small yields only of non-phosphorus-containing heterocyclic compounds. Observation of the reactions by n. m. r. spectroscopy, however, showed that 3, 4-diaryl -4, 5-dihydro-1, 2, 5-oxazaphosph(v)ole-2-oxides were formed, and subsequently decomposed, under the reaction conditions. The use of t-butanol as solvent for the reaction enabled a range of novel 4, 5-dihydro-1, 2, 5-oxazaphosph(v)ole -2- oxides to be prepared and isolated at room temperature. The reaction was extended by the use of dimethyl phenylphosphonite and 2-phenyl-1, 3, 2-dioxaphospholan, instead of trialkyl phosphites.

Further investigations, of the thermolysis of the 1, 2, 5-oxazaphosph(v)ole-2-oxides and their reactions with tervalent phosphorus reagents, suggested that the compounds were not intermediates in the formation of the non -phosphorus- containing heterocycles isolated previously. The results suggested that the reaction of a tervalent phosphorus reagent with a 2-aryl-1-phenyl-1-nitroethene involves two competing pathways:- Michael-type addition of the phosphorus reagent to the nitroethene, with the possibility of subsequent ring-closure to give a 4, 5-dihydro-1, 2, 5-oxazaphosph(v)ole-2-oxide, or deoxygenation of the nitro-group to give a vinyl nitrene, and hence nitrene-derived products.

The thermolyses of two aryl 2-azidophenyl ethers in triethyl phosphate were found to give significantly different yields of products than the corresponding reactions in decalin. The possible formation of a zwitterionic nitrene-phosphate adduct as a reactive intermediate seems to be insufficient explanation of the observed results.

Reaction of N-t-butylphenylnitroxyl and diphenylnitroxyl with triethyl phosphite, in ethanol or methanol saturated with lithium chloride, gave ring-chlorinated anilines. This was taken as evidence in support of a reaction mechanism in which pairs of aminyl radicals undergo an electron-transfer reaction to give an anilino-anion and a delocalised nitrenium ion, which readily undergoes nucleophilic aromatic substitution by the solvent or chloride ion.

The decomposition of 1, 4-di-t-butyl-1, 4-bisphenyltetraz-2-ene in ethanol or methanol also gave ring- substituted N-t -but ylanilines.

http://hdl.handle.net/1842/33411

The University of Edinburgh

Annexe Thesis Digitisation Project 2019 Block 22

Reactions of phosphorus (III) reagents with nitro compounds and nitroxyls

Thesis or Dissertation

Doctoral

PhD Doctor of Philosophy