Phenyl acetate

Not to be confused with phenylacetate, the conjugate base of phenylacetic acid.
Phenyl acetate
Skeletal formula of phenyl acetate
Ball-and-stick model of the phenyl acetate molecule
Names
IUPAC name
Phenyl ethanoate
Other names
Phenol acetate; (Acetyloxy)benzene; Acetoxybenzene
Identifiers
122-79-2 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:8082 YesY
ChemSpider 28969
ECHA InfoCard 100.004.160
PubChem 31229
Properties
C8H8O2
Molar mass 136.15 g·mol−1
Density 1.075 g/mL[1]
Melting point 50 °C (122 °F; 323 K)
Boiling point 195–196 °C (383–385 °F; 468–469 K)[1]
Hazards
Flash point 76 °C (169 °F; 349 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Phenyl acetate is the ester of phenol and acetic acid. One way that it can be produced by decarboxylation of aspirin. Another way that it can be produced is by reacting phenol with acetic anhydride.

Phenyl acetate can be separated into phenol and an acetate salt, via saponification: heating the phenyl acetate with a strong base, such as sodium hydroxide, will produce phenol and sodium acetate. The two chemicals can then be separated by heat and decantation or heat and filtration.

References

This article is issued from Wikipedia - version of the 12/20/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.