Fluoroacetyl chloride
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Names | |||
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Preferred IUPAC name
Fluoroacetyl chloride | |||
Other names
2-Fluoroacetyl chloride Fluoroethanoyl chloride | |||
Identifiers | |||
359-06-8 = | |||
3D model (Jmol) | Interactive image | ||
ChemSpider | 9282 | ||
ECHA InfoCard | 100.006.022 | ||
PubChem | 9663 | ||
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Properties | |||
C2H2ClFO | |||
Molar mass | 96.49 g·mol−1 | ||
Boiling point | 70 to 71 °C (158 to 160 °F; 343 to 344 K) at 755 mmHg[1] | ||
Hazards | |||
NFPA 704 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
Fluoroacetyl chloride is an acyl chloride.
In 1948, William E. Truce of Purdue University described a synthesis of fluoroacetyl chloride which was undertaken "because of its potential value for introducing the group, —COCH2F, into organic molecules."[1] In this synthesis, he reacted sodium fluoroacetate with phosphorus pentachloride to obtain the desired compound.
References
- 1 2 Truce, William E. (August 1948). "The Preparation of Fluoroacetyl Chloride". Journal of the American Chemical Society. 70 (88): 2828–2828. doi:10.1021/ja01188a524.
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