Réaction #451857

Équation de réaction

chloroform

2-carbomethoxy-7-oxabicyclo(2,2,1)hept-5-ene

stearylamine

hydrochloric acid

→

N-stearylacrylamide

Solvants

water

Conditions de réaction

Traitement

1. 1
   Autrethe organic phase is separated off
2. 2
   Extractionthe aqueous phase extracted with 50 parts chloroform
3. 3
   AutreThe combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C. under a vacuum of 20 Torr
4. 4
   TempératureThe residue is heated in a vacuum to 110° to 120° C. (bath temperature 140° C.)
5. 5
   AutreAt the conclusion of the furane separation
6. 6
   Températurethe sedimentation temperature increases to 140° C
7. 7
   TempératureThe mixture is cooled down
8. 8
   workup.DISSOLUTIONthe product is dissolved in hot acetone
9. 9
   Filtrationfiltered
10. 10
    Autreto recrystallise

Mode opératoire

7.2 parts 30% methanolic Na-methylate solution and 77 parts 2-carbomethoxy-7-oxabicyclo(2,2,1)hept-5-ene are added to 134.8 parts stearylamine. The reaction medium is heated to 60° C. and stirred for 15 hours at this temperature. 300 parts of chloroform are next added and the mixture neutralised with 4 parts concentrated hydrochloric acid. 100 parts of water are added, the organic phase is separated off, and the aqueous phase extracted with 50 parts chloroform. The combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C. under a vacuum of 20 Torr. The residue is heated in a vacuum to 110° to 120° C. (bath temperature 140° C.). At the conclusion of the furane separation, the sedimentation temperature increases to 140° C. The mixture is cooled down, the product is dissolved in hot acetone, filtered, and allowed to recrystallise. 117 parts N-stearylacrylamide having a melting point of 75° to 77° C. are obtained.

Source