Reaktion #95092

Reaktionsgleichung

trans-2-(4-nitrophenyl)cyclopropanecarboxylic acid

octylamine

ethyl chloroformate

→

title compound

trans-N-Octyl-2-(4-nitrophenyl)-cyclopropanecarboxamide

Lösungsmittel

chloroform

chloroform

triethylamine

chloroform

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe clear solution thus obtained
2. 2
   workup.STIRRINGStirring
3. 3
   workup.WAITwas continued for 20 minutes
4. 4
   workup.STIRRINGwith stirring, at 0°-5° C., during 10-15 minutes
5. 5
   SonstigeThe cooling bath was removed
6. 6
   workup.STIRRINGstirring
7. 7
   workup.WAITwas continued for 1 hour
8. 8
   SonstigeAt this point, the solvent was removed by evaporation in vacuo
9. 9
   Sonstigethe residue was triturated under a mixture of 70 ml
10. 10
    Filtrationwas recovered by filtration
11. 11
    Waschenwashed with water
12. 12
    Sonstigedried
13. 13
    Sonstigeto give 6.2 g

Vorschrift

To a stirred slurry of 4.1 g. of trans-2-(4-nitrophenyl)cyclopropanecarboxylic acid in 50 ml. of chloroform was added 2.2 g. of triethylamine. The clear solution thus obtained was cooled to ca. 5° C., and a solution of 2.4 g. of ethyl chloroformate in 15 ml. of chloroform was added dropwise with stirring during 15 minutes. Stirring was continued for 20 minutes, and then a solution of 2.8 g. of octylamine in 15 ml. of chloroform was added dropwise with stirring, at 0°-5° C., during 10-15 minutes. The cooling bath was removed, and stirring was continued for 1 hour. At this point, the solvent was removed by evaporation in vacuo, and the residue was triturated under a mixture of 70 ml. of water and 15 ml. of ethanol. The solid which remained out of solution was recovered by filtration, washed with water, and dried, to give 6.2 g. of the title compound as a white solid, m.p. 126° -129° C.

Quelle