Pages

Sunday, June 2, 2019

SYNTHESIS OF PENTYLBENZENE (1-Phenylpentane)



  • In a 1500-ml three-necked flask equipped with a dropping funnel, a sealed stirrer unit and a double surface condenser to which is attached a guard-tube filled with a mixture of calcium chloride and soda-lime, prepare an ethereal solution of benzylmagnesium chloride from 24.3 g (1 mol) of clean, dry magnesium turnings (under 100 ml of anhydrous ether) and a solution of 126.5g (115 ml, 1 mol) of freshly distilled benzyl chloride in 500 ml of anhydrous ether. 
  • Use a crystal of iodine as a catalyst. 
  • Finally, cool the flask by immersion in a bath of ice-water. 
  • Place a solution of 456g (2 mol) of butyl toluene-p-sulphonate in about twice the volume of anhydrous ether in the dropping funnel, and add it slowly to the vigorously stirred benzylmagnesium chloride solution, at such a rate that the ether just boils; a white solid soon forms. 
  • The addition is complete after about 2 hours. 
  • Pour the reaction product slowly into a mechanically stirred mixture of 1 kg of finely crushed ice, 1 litre of water and 125 ml of concentrated hydrochloric acid contained in a 4- or 5-litre beaker; the precipitated magnesium toluene-p-sulphonate will ultimately pass into the solution. 
  • Separate the ether layer, extract the aqueous layer with 250 ml of ether and wash the combined ether solutions with about 100 ml of water. 
  • Dry the ether solution with about 10g of anhydrous potassium carbonate. 
  • Distil off the ether on a rotary evaporator, add to the mixture 5-7g of sodium cut into small pieces and heat under reflux for about 2 hours in order to remove any benzyl alcohol which may have formed by atmospheric oxidation of benzylmagnesium chloride. 
  • Decant the solution and distil it from an air bath through a well-lagged and efficient fractionating column; collect the fraction, b.p. 190-210 °C. 
  • Redistil and collect the pentylbenzene at 198-203 °C. The yield is 90 g (61%). 
  • Record the i.r. spectrum and the p.m.r. spectrum and assign the absorptions using the spectra quoted above for butulbenzene a guide. Interpret the m.s. which shows principal fragment ions at m/z 148, 105, 91, 77 and 65.



No comments:

Post a Comment

We specialize in producing high value chemicals. Besides our regular products, we strive to develop new products based on customer’s requirements. Our R&D center plays crucial role in handling complex chemistries and developing newer technologies. We respect intellectual property rights and have confidentiality agreement with various multi national companies. We undertake contract manufacturing of fine chemicals and advance intermediates of API’s.