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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66814Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/66814

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOctylamineHCID 8143—
EduktEthyl chloroformateHCID 10928—
Eduktrac-(1R,2R)-2-(4-nitrophenyl)cyclopropane-1-carboxylic acidHCID 12854631—
LösungsmittelChloroformHCID 6212—
LösungsmittelTriethylamineHCID 8471—
Produkttrans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamideHCID 12854633—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343813
Quelldatensatzuspto-grants-1982_08
ORD IDord-392ee65cf4244ebc867e6abbcd49cb68
Quellennotizuspto-grants-1982_08