3-Methyl-3-pentanol

3-Methyl-3-pentanol (IUPAC name: 3-methylpentan-3-ol) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate.[2]

3-Methyl-3-pentanol[1]
Names
Preferred IUPAC name
3-Methylpentan-3-ol
Other names
3-Methyl-3-pentanol
Diethyl carbinol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.959
EC Number
  • 201-053-4
UNII
Properties
C6H14O
Molar mass 102.174 g/mol
Appearance colorless liquid
Odor fruity
Density 0.8286 g/cm3 at 20 °C
Melting point −23.6 °C (−10.5 °F; 249.6 K)
Boiling point 122.4 °C (252.3 °F; 395.5 K)
45 g/L
Solubility miscible with ethanol, diethyl ether
Thermochemistry
293.4 J·mol−1·K−1 (liquid)
Hazards
Safety data sheet http://www.sciencelab.com/msds.php?msdsId=9926087
GHS pictograms
GHS Signal word Warning
GHS hazard statements
H226, H302
P210, P233, P240, P241, P242, P243, P264, P270, P280, P301+312, P303+361+353, P330, P370+378, P403+235, P501
Lethal dose or concentration (LD, LC):
710 mg/kg rat
Related compounds
Related compounds
Hexanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Synthesis

It can be prepared by reacting ethylmagnesium bromide with methyl acetate in the so-called Grignard reaction using dried diethyl ether or tetrahydrofuran as solvent.

Synthesis of 3-Methyl-3-pentanol

It can be prepared also by reacting ethylmagnesium bromide with butanone in the same conditions already mentioned.

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References

  1. Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 3–400, 5–47, 8–106, ISBN 0-8493-0594-2
  2. Sittig, Marshall (1988), Pharmaceutical manufacturing encyclopedia, 2 (2 ed.), William Andrew, pp. 555–556, ISBN 978-0-8155-1144-1, retrieved 2010-01-22


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