A | B | C | D | E | F | G | H | CH | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9
Names | |
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Preferred IUPAC name
1,1,1,3,3,3-Hexafluoro-2-(trifluoromethyl)propan-2-ol | |
Other names
perfluoro-tert-butyl alcohol, perfluoro-tert-butanol
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.017.417 |
EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C4F9OH | |
Molar mass | 236.04 g/mol |
Appearance | Colorless liquid |
Boiling point | 45 °C (113 °F; 318 K) |
Miscible | |
Acidity (pKa) | 5.4 (in H2O) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Corrosive, eye irritant |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Nonafluoro-tert-butyl alcohol (IUPAC name: 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol) is a fluoroalcohol. It is the perfluorinated analog of tert-butyl alcohol. Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a pKa value of 5.4, similar to that of a carboxylic acid. As another consequence of being a perfluorinated compound, it is also one of the lowest boiling alcohols, with a boiling point lower than that of methanol.
Synthesis
It is prepared by addition of trichloromethyllithium to hexafluoroacetone, followed by halogen exchange with antimony pentafluoride.[1] The aluminate derived from its alkoxide anion, tetrakisaluminate(1–), {Al4}– is used as a weakly coordinating anion.[2]
See also
- 2,2,2-Trifluoroethanol
- 1,1,1,3,3,3-Hexafluoro-2-propanol
- Hexafluoroacetone
- Perfluorotriethylcarbinol
References
- ^ Filler, Robert; Schure, Ralph M. (1967-04-01). "Highly acidic perhalogenated alcohols. A new synthesis of perfluoro-tert-butyl alcohol". The Journal of Organic Chemistry. 32 (4): 1217–1219. doi:10.1021/jo01279a081. ISSN 0022-3263.
- ^ Krossing, Ingo; Raabe, Ines (2004-04-13). "Noncoordinating Anions—Fact or Fiction? A Survey of Likely Candidates". Angewandte Chemie International Edition. 43 (16): 2066–2090. doi:10.1002/anie.200300620. ISSN 1433-7851. PMID 15083452.
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