تفاعل #160996

ord-65d86b4b9a294a3eb4681ff2ad2ec308

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe limitations of conventional synthesis methods
  2. 2
    أخرىThe round bottom is fitted with a Dean-Stark trap and condenser
  3. 3
    درجة الحرارةto reflux
  4. 4
    درجة الحرارةHeating
  5. 5
    أخرى(1 hr)
  6. 6
    درجة الحرارةThe mixture is cooled
  7. 7
    workup.ADDITIONpoured into a separatory funnel
  8. 8
    غسيلThe solution is washed twice with 50 mL of saturated sodium bicarbonate solution and once with 50 mL of distilled water
  9. 9
    تجفيفThe organics are dried over MgSO4
  10. 10
    workup.DISTILLATIONthe residue distilled
  11. 11
    أخرىA fraction collected at 150° C.

الإجراء التجريبي

This example illustrates the limitations of conventional synthesis methods. A 500 mL round bottom is charged with 191 g normal butyraldehyde, 101 g of 1,3-propanediol, and 4 drops 85% phosphoric acid. The round bottom is fitted with a Dean-Stark trap and condenser and the entire apparatus is placed into an electric heating mantle and brought to reflux. The aldehyde/water azeotrope condenses and separates into the trap. Heating is maintained until 24 mL of water has evolved (1 hr). The mixture is cooled and poured into a separatory funnel. The solution is washed twice with 50 mL of saturated sodium bicarbonate solution and once with 50 mL of distilled water. The organics are dried over MgSO4 and the residue distilled. A fraction collected at 150° C. is 99.6% acetal and has a mass of 95.7 g. This corresponds to a yield of 56%, lower than the yields reported in Table II.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08829207B2uspto-grants-2014_09