Chemistry:Methyl bisulfate

From HandWiki
Methyl bisulfate
Skeletal formula
Ball-and-stick model
  Sulfur, S
  Oxygen, O
  Carbon, C
  Hydrogen, H
Names
Preferred IUPAC name
Methyl hydrogen sulfate
Systematic IUPAC name
Methoxysulfonic acid
Other names
  • Methyl sulfate
  • Metilsulfate
  • Methylsulfuric acid
  • Monomethyl sulfate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
EC Number
  • 201-058-1
KEGG
UNII
Properties
(CH
3)HSO
4
Molar mass 112.10 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references
Tracking categories (test):

Methyl bisulfate is a chemical compound with the molecular formula (CH
3)HSO
4. This compound is the mono-methyl ester of sulfuric acid. Its structure is CH
3–O–S(=O)
2–OH. The significance of methyl bisulfate is that it is an intermediate in the hydrolysis of the important reagent dimethyl sulfate, (CH
3)
2SO
4:[1]

(CH
3)
2SO
4 + H
2O → (CH
3)HSO
4 + CH
3OH

Methyl bisulfate is a strong acid:

(CH
3)HSO
4 → (CH
3)SO−
4 + H+

Methyl bisulfate came into the public view in 1993 with the discovery that certain mercury compounds catalyze the conversion of methane to methylbisulfate in good yields with excellent selectivity in concentrated sulfuric acid.[2] However, because of the toxicity and concerns with the use of mercury it wasn't until 1998 when platinum complexes were found that catalyze the reaction of CH
4 by SO
3 and O
2 that it came into the limelight:[3][4][5]

2 CH
4 + 2 SO
3 + O
2 → 2 (CH
3)HSO
4

This discovery pointed to a possible method for upgrading inexpensive and abundantly available methane (natural gas) into methanol, which is both a more useful chemical and more easily shipped than methane. The process is proposed to proceed via an intermediate containing the Pt–CH
3 group.[6]

Methyl bisulfate's conjugate base is used as a counterion in the formulation of some pharmaceutical drugs, where it is typically referred to as metilsulfate.[7]

References

  1. ↑ Robertson, R. E.; Sugamon, S.E. (1966). "The Hydrolysis of Dimethyl Sulfate and Diethyl Sulfate in Water". Canadian Journal of Chemistry 44 (14): 1728–1730. doi:10.1139/v66-260. 
  2. ↑ Periana, R.A.; Taube, D.J.; Evitt, E.R.; Loffler, D.G.; Wentrcek, P.R.; Voss, G.; Masuda, T. (1993). "A Mercury-Catalyzed, High-Yield System for the Oxidation of Methane to Methanol". Science 259 (5093): 340–343. doi:10.1126/SCIENCE.259.5093.340. PMID 17832346. 
  3. ↑ Hristov, I. H.; Ziegler, T. (2003). "The Possible Role of SO3 as an Oxidizing Agent in Methane Functionalization by the Catalytica Process. A Density Functional Theory Study". Organometallics 22 (8): 1668–1674. doi:10.1021/om020774j. 
  4. ↑ Periana, R. A.; Mirinov, O.; Taube, D. J.; Gamble, S (2002). "High Yield Conversion of Methane to Methyl Bisulfate Catalyzed by Iodine Cations". Chemical Communications (20): 2376–2377. doi:10.1039/b205366g. 
  5. ↑ Wolf, D. (1999). "High Yields of Methanol from Methane by C-H Bond Activation at Low Temperatures". Angewandte Chemie International Edition 37 (24): 3351–3353. doi:10.1002/(SICI)1521-3773(19981231)37:24<3351::AID-ANIE3351>3.0.CO;2-U. 
  6. ↑ Periana, R. A.; Taube, D. J.; Gamble, S.; Taube, H.; Satoh, T.; Fujii, H. (1998). "Platinum Catalysts for the High-Yield Oxidation of Methane to a Methanol Derivative". Science 280 (5363): 560–564. doi:10.1126/science.280.5363.560. PMID 9554841. 
  7. ↑ International nonproprietary names (INN) for pharmaceutical substances. World Health Organization. 



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Methyl_bisulfate&oldid=3325116"