Acetyl nitrate

Acetyl nitrate
Names
Preferred IUPAC name
Acetic nitric anhydride
Other names
Acetyl nitrate
Identifiers
CAS Number
  • 591-09-3 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 11069
PubChem CID
  • 11557
UNII
  • 79CY6496CR checkY
CompTox Dashboard (EPA)
  • DTXSID40207839 Edit this at Wikidata
InChI
  • InChI=1S/C2H3NO4/c1-2(4)7-3(5)6/h1H3
    Key: JCZMXVGQBBATMY-UHFFFAOYSA-N
  • CC(=O)O[N+](=O)[O-]
Properties
Chemical formula
C2H3NO4
Molar mass 105.049 g·mol−1
Appearance colorless liquid
Density 1.24 g/cm3 (15 °C)
Boiling point 22 °C at 70 Torr[1]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
explosion
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Acetyl nitrate is the organic compound with the formula CH3C(O)ONO2. It is classified as the mixed anhydride of nitric and acetic acids. It is a colorless explosive liquid that fumes in moist air.

Synthesis and reactions

It was first prepared in 1907 by Amé Pictet and E. Khotynsky from acetic anhydride and dinitrogen pentoxide, fuming nitric acid can also be used:

(CH3CO)2O + HNO3 → CH3C(O)ONO2 + CH3COOH

It hydrolyzes in moist air to acetic acid and nitric acid. Alternatively, nitric acid adds to ketene.

It is used for some nitrations and nitrolysis reactions.[2] It acetylates amines, akin to the behavior of acetyl chloride:

2 NH 3 + CH 3 C ( O ) ONO 2 NH 4 NO 3 + CH 3 CONH 2 {\displaystyle {\ce {2NH3 + CH3C(O)ONO2 -> NH4NO3 + CH3CONH2}}}

References

  1. ^ A. Pictet, E. Khotinsky: Über Acetylnitrat. in Chem. Ber. 40, 1907, S. 1163–1166, doi:10.1002/cber.190704001172.
  2. ^ Louw, Robert "Acetyl nitrate" e-EROS Encyclopedia of Reagents for Organic Synthesis 2001, 1-2. doi:10.1002/047084289X.ra032