Pages

Friday, August 10, 2018

SYNTHESIS OF HEPTANOIC ANHYDRIDE



CAUTION: All operations should be conducted in an efficient fume cupboard owing to the toxicity of pyridine and benzene.

  • In a 250-ml, round-bottomed three-necked flask, provided with a dropping funnel, stirrer and thermometer, place 15.8g (16.1ml, 0.2 mol) of dry pyridine and 25 ml of dry benzene. 
  • Stir and add rapidly 14.8g (15.5 ml, 0.1 mol) of heptanoyl chloride; the temperature rises slightly and a pyridinium complex separates. 
  • Introduce 13.0g (14.1ml, 0.1 mol) of heptanoic acid with stirring, over a period of 5 minutes; the temperature rises to 60-65 °C and pyridine hydrochloride is formed. 
  • Continue the stirring for 10 minutes and collect the hygroscopic pyridine hydrochloride as rapidly as possible on a chilled Buchner or sintered glass funnel, and wash it with two 25-ml portions of dry benzene. 
  • Remove the benzene from the filtrate under reduced pressure on a water bath, and distil the residue through a short fractionating column. 
  • Collect the heptanoic anhydride at 170-173 °C/15mmHg; the yield is 20g (83%).





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.