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30th August 2013 @ 15:49

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Reaction information

*#Reaction file
*Reaction file type CDX

To a solution of ZrCp2Cl2 (321 mg, 1.1 mmol) in THF (5 mL) at –80 °C under Ar is added dropwise n-butyllithium (0.88 mL of a 2.5 M solution in hexanes, 2.2 mmol). In the case of substrates containing a free hydroxyl group, 2.2 equivalents of ZrCp2Cl2 (642 mg) and 4.4 equivalents of n-butyllithium (1.76 mL) are used. After the addition of butyllithium, a solution of the 2-(4-pentenyl)-4,5-dihydrofuran (331 mg, 2.4 mmol) in THF (2 mL) is added dropwise and the solution allowed to warm to RT. After between 3 h and 16 h at RT, MeOH (3 mL) and saturated NaHCO3 solution (7 mL) are added and the cloudy white or pale yellow reaction mixture stirred for between 2 h and 16 h. After dilution of the reaction mixture with ether (20 mL) and water (20 mL), the aqueous phase is separated and extracted with ether (3 x 50 mL). The combined organic phases are combined and washed with brine, dried over MgSO­4, filtered and concentrated. The crude oil was purified by column chromatography (SiO2, 25% ether in petrol) to give the desired product as a clear, colourless oil (263 mg, 78%).

*Yield (%) 78
*Type of Yield Isolated Product Yield 

E. Negishi, F. E. Cederbaum, T. Takahashi, Tetrahedron Lett. 1986, 27, 2829.

Further information Compound 307: 3-(2-(E)-Methylcyclopentyliden)-1-propanol 

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 
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