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Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents

[Image: see text] While the use of triphenylphosphine as a reductant is common in organic synthesis, the resulting triphenylphosphine oxide (TPPO) waste can be difficult to separate from the reaction product. While a number of strategies to precipitate TPPO are available, none have been reported to...

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Autores principales: Batesky, Donald C., Goldfogel, Matthew J., Weix, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634519/
https://www.ncbi.nlm.nih.gov/pubmed/28956444
http://dx.doi.org/10.1021/acs.joc.7b00459
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author Batesky, Donald C.
Goldfogel, Matthew J.
Weix, Daniel J.
author_facet Batesky, Donald C.
Goldfogel, Matthew J.
Weix, Daniel J.
author_sort Batesky, Donald C.
collection PubMed
description [Image: see text] While the use of triphenylphosphine as a reductant is common in organic synthesis, the resulting triphenylphosphine oxide (TPPO) waste can be difficult to separate from the reaction product. While a number of strategies to precipitate TPPO are available, none have been reported to work in more polar solvents. We report here that mixing ZnCl(2) with TPPO precipitates a TPPO–Zn complex in high yield in several common polar organic solvents. The solvent compatibility of this procedure and the reliability of the precipitation in the presence of polar functional groups were examined to show the utility and limitations of this method.
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spelling pubmed-56345192017-10-11 Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents Batesky, Donald C. Goldfogel, Matthew J. Weix, Daniel J. J Org Chem [Image: see text] While the use of triphenylphosphine as a reductant is common in organic synthesis, the resulting triphenylphosphine oxide (TPPO) waste can be difficult to separate from the reaction product. While a number of strategies to precipitate TPPO are available, none have been reported to work in more polar solvents. We report here that mixing ZnCl(2) with TPPO precipitates a TPPO–Zn complex in high yield in several common polar organic solvents. The solvent compatibility of this procedure and the reliability of the precipitation in the presence of polar functional groups were examined to show the utility and limitations of this method. American Chemical Society 2017-09-28 2017-10-06 /pmc/articles/PMC5634519/ /pubmed/28956444 http://dx.doi.org/10.1021/acs.joc.7b00459 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Batesky, Donald C.
Goldfogel, Matthew J.
Weix, Daniel J.
Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title_full Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title_fullStr Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title_full_unstemmed Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title_short Removal of Triphenylphosphine Oxide by Precipitation with Zinc Chloride in Polar Solvents
title_sort removal of triphenylphosphine oxide by precipitation with zinc chloride in polar solvents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634519/
https://www.ncbi.nlm.nih.gov/pubmed/28956444
http://dx.doi.org/10.1021/acs.joc.7b00459
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