Jump to content
Wikipedia The Free Encyclopedia

Fluorocyclopropane

From Wikipedia, the free encyclopedia
Fluorocyclopropane
Names
Preferred IUPAC name
Fluorocyclopropane
Other names
Cyclopropyl fluoride, cyclopropylfluoride
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 212-459-6
  • InChI=1S/C3H5F/c4-3-1-2-3/h3H,1-2H2
    Key: XAVRRVJJYIFROR-UHFFFAOYSA-N
  • C1CC1F
Properties
C3H5F
Molar mass 60.071 g·mol−1
Density g/cm3
Insoluble
Related compounds
Related compounds
Chlorocyclopropane
Bromocyclopropane
Iodocyclopropane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Fluorocyclopropane is an organofluorine compound with the chemical formula C3H5F. The compound is a member of haloalkane family.[1]

Synthesis

[edit ]

The compound can be produced by reacting imidazolylidene cyclopropyl group with xenon difluoride.[2]

Also, a reaction of enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids.[3]

See also

[edit ]

References

[edit ]
  1. ^ Kerr, J. A.; Kirk, A. W.; O'Grady, B. V.; Phillips, D. C.; Trotman-Dickenson, A. F. (1967). "Kinetics of decomposition of chemically activated alkyl fluorides". Discussions of the Faraday Society . 44: 263. doi:10.1039/DF9674400263 . Retrieved 29 May 2023.
  2. ^ Mankad, Neal P.; Toste, F. Dean (2012). "C(sp 3 )–F reductive elimination from alkylgold( iii ) fluoride complexes". Chem. Sci. 3 (1): 72–76. doi:10.1039/C1SC00515D. PMC 3474378 . Retrieved 29 May 2023.
  3. ^ Delion, Laëtitia; Poisson, Thomas; Jubault, Philippe; Pannecoucke, Xavier; Charette, André B. (September 2020). "Synthesis of fluorocyclopropanes via the enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids". Canadian Journal of Chemistry . 98 (9): 516–523. doi:10.1139/cjc-2020-0036. ISSN 0008-4042 . Retrieved 29 May 2023.

Extra reading

[edit ]
  • Dall'O, L.; Heydtmann, H. (January 1987). "Kinetic Study of Chemically Activated Fluorocyclopropane". Berichte der Bunsengesellschaft für physikalische Chemie. 91 (1): 24–30. doi:10.1002/bbpc.19870910107.
  • Casas, F.; Kerr, J. A.; Trotman-Dickenson, A. F. (1964). "706. Fluorinated cyclopropanes. Part II. The thermal isomerization of monofluorocyclopropane". Journal of the Chemical Society (Resumed): 3655. doi:10.1039/JR9640003655.
Salts and covalent derivatives of the fluoride ion
HF ?HeF2
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
PF6, AsF6, SbF6 compounds
AlF2−5, AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl

AltStyle によって変換されたページ (->オリジナル) /