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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26251생성일: 2026년 10월 27일

Triethylamine → trans-N-[2-(Dimethylamino)cyclohexyl]alpha,alpha,alpha-trifluoro-p-toluamide

https://huagongshe.com/reaction/26251

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
반응물N1,N1-dimethylcyclohexane-1,2-diamineHCID 12447266—
생성물trans-N-[2-(Dimethylamino)cyclohexyl]alpha,alpha,alpha-trifluoro-p-toluamideHCID 53682390—

반응 단계

The titled amide was prepared according to general procedure B using p-trifluoromethyl-benzoyl chloride (4.17 g.; 0.02 mole), N,N-dimethylcyclohexane-1,2-diamine (2.84 g.; 0.02 mole) and triethylamine (2.02 g., 0.02 mole). The crude solid was crystallized from ether to give 4.766 g. (77% yield) of colorless needles, m.p. 141°-142°, raised to 141.5°-142.5° on recrystallization. uv λmax 222 nm (ε 11,450), sh 245 (5,550); sh 260 (3,400); sh 276 (1.750). ir NH 3310; =CH 3030; N-alkyl 2770, 2740; C=O 1635; C=O 1575, 1510; amide II 1550; CF3 /ether 1330, 1190, 1165, 1130, 1105, 1065, 1020; aromatic 860; nmr in CDCl3 at 100 MHz was in accord. Mass spectrum M+ 314.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148914
출처 데이터셋uspto-grants-1979_04
ORD IDord-6a868260414a4df599a3e4b8bdb3c653
출처 메모uspto-grants-1979_04