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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66814생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물OctylamineHCID 8143—
반응물Ethyl chloroformateHCID 10928—
반응물rac-(1R,2R)-2-(4-nitrophenyl)cyclopropane-1-carboxylic acidHCID 12854631—
용매ChloroformHCID 6212—
용매TriethylamineHCID 8471—
생성물trans-N-Octyl-2-(4-nitrophenyl)cyclopropanecarboxamideHCID 12854633—

반응 조건

온도5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04343813
출처 데이터셋uspto-grants-1982_08
ORD IDord-392ee65cf4244ebc867e6abbcd49cb68
출처 메모uspto-grants-1982_08