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2nd September 2013 @ 13:21

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Reaction information

*#Reaction file
ReactionScheme.cdx
 
*Reaction file type CDX 
*Procedure

To a solution of ethyl vinyl ether (0.95 mL, 721 mg, 10 mmol) in THF (8 mL) at –70 °C under Ar is added dropwise tert-butyllithium (4.7 mL of a 1.7 M solution in pentanes, 8 mmol), resulting in a bright yellow suspension. The reaction is allowed to warm, resulting in dissolution of the yellow precipitate, and disappearance of the yellow colour at around 0 °C. The solution is re-cooled to –70 °C and a solution of the 2,2-dimethyl-4-penten-1-al (336 mg, 3 mmol) in THF (2 mL) is added. After warming to 0 °C and stirring for between 1 h and 5 h, saturated NH4Cl solution (10 mL) is added. After dilution with ether (20 mL), the aqueous phase is separated and extracted with ether (3 x 50 mL), and the combined organic phases washed with brine, dried over Na2SO4, filtered and concentrated. The crude product was purified by Kugelrohr distillation (110 °C, 1.0 mbar), yielding a clear, colourless oil (414 mg, 75%). 

*Yield (%) 75 
*Type of Yield Isolated Product Yield 
Reference(s)
DavidOwenThesis2000pp49,119.pdf
330LABBOOK.JPG
 
Further information Compound 330: 4,4-Dimethyl-2-ethoxy-3-hydroxy-1,6-heptadiene 

For multistep reactions (or their steps):

Overall reaction? True 
For overall reaction - links to child reaction steps N/A 
For step in multistep reaction - link to previous reaction step N/A 
For step in multistep reaction - link to following reaction step N/A 
Attached Files
ReactionScheme.gif
ReactionScheme.cdx
DavidOwenThesis2000pp49,119.pdf
330LABBOOK.JPG