Pyridinium p-toluenesulfonate

Pyridinium p-toluenesulfonate (PPTS) is a colourless solid salt of pyridine and p-toluenesulfonic acid.

Pyridinium p-toluenesulfonate
Names
IUPAC name
4-methylbenzenesulfonate; pyridin-1-ium
Other names
pyridinium p-toluenesulfonate
Identifiers
3D model (JSmol)
Abbreviations PPTS
ChemSpider
ECHA InfoCard 100.041.806
  • InChI=1S/C7H8O3S.C5H5N/c1-6-2-4-7(5-3-6)11(8,9)10;1-2-4-6-5-3-1/h2-5H,1H3,(H,8,9,10);1-5H Y
    Key: ZDYVRSLAEXCVBX-UHFFFAOYSA-N Y
  • InChI=1/C7H8O3S.C5H5N/c1-6-2-4-7(5-3-6)11(8,9)10;1-2-4-6-5-3-1/h2-5H,1H3,(H,8,9,10);1-5H
    Key: ZDYVRSLAEXCVBX-UHFFFAOYAE
  • CC1=CC=C(S(=O)([O-])=O)C=C1.C2=[NH+]C=CC=C2
Properties
C12H13NO3S
Molar mass 251.30 g·mol−1
Appearance Colourless solid
Melting point 120 °C (248 °F; 393 K) source[1]
Acidity (pKa) 5.21[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Uses

In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C5H5NH+) ions. For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts. It is also a commonly used catalyst for the preparation of acetals and ketals from aldehydes and ketones.

References
  1. TOKYO CHEMICAL INDUSTRY CO., LTD. "Pyridinium p-Toluenesulfonate". Retrieved 2011-09-16.
  2. David A. Evans (2005-11-04). "Evans pKa Table" (PDF). Retrieved 2016-03-02.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.