PMGB

chemical reaction procedures

Reduction of esters

with 2 comments

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A mixture of the ester (0.022 mol) and sodium borohydride (0.039 mol) in 250 mL anhydrous ethanol was refluxed for overnight (12 h). The reaction mixture was concentrated, the semi solid residue was diluted with 250 mL of dichloromethane, washed with 250 mL of saturated aqueous NaHCO3 solution, dried (Na2SO4) and evaporated under reduced pressure to give the corresponding alcohol which was purified by silica gel column chromatography (using a gradient of hexane and ethyl acetate) followed by triturating with ether (white solid, 22% yield).

1H NMR (400 MHz, CDCl3): d 2.40 (t, J = 7.6 Hz, 2H); 2.81 (t, J = 7.2 Hz, 2H); 4.38 (d, J = 5.6 Hz, 2H); 5.11 (t, J = 5.6 Hz, 1H); 6.80-6.82 (m, 2H); 7.06 (d, J = 8.0 Hz, 1H); 10.04 (s, 1H).

 

 

 

 

 

Written by pmgb

March 21, 2008 at 5:39 am

Posted in alcohols, esters

2 Responses

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  1. low yield is due to side products arising from reduction of an internal amide bond

    pmgb

    March 21, 2008 at 7:46 am

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    james

    January 21, 2009 at 11:15 am


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