돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502735생성일: 2026년 10월 26일

Triethylamine → N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/502735

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물2-MorpholinoethylamineHCID 408285—
반응물3-Nitro-5-(trifluoromethyl)benzoic acidHCID 616602—
용매DichloromethaneHCID 6344—
생성물N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamideHCID 59427894—

반응 조건

온도75 °C

반응 단계

A mixture of 3-nitro-5-(trifluoromethyl)benzoic acid (300 mg, 1.29 mmol, 1.0 equiv) and thionyl chloride (2.0 ml) was heated at 75° C. for 1 h. The solvent was removed in vacuo and the residue taken up in CH2Cl2 (5.0 ml). To the solution was added 2-morpholinoethanamine (185 mg, 1.42 mmol, 1.1 equiv) and triethylamine (0.54 ml, 3.86 mmol, 3.0 equiv). After the reaction was complete, the solution was diluted with CH2Cl2 (ca. 10 ml) and washed with water and brine. After drying with Na2SO4 and concentration in vacuo, the resulting N-(2-morpholinoethyl)-3-nitro-5-(trifluoromethyl)benzamide was advanced without further purification. MS m/z: 348 (M+H+); Calculated for C14H16F3N3O4: 347.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776869B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-355fa31aa4ef4b6dba3fbca6b79af093
출처 메모uspto-grants-2010_08