돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968279생성일: 2026년 10월 24일

N-Ethylaniline → N-ethyl-2-iodo-4-nitro-N-phenyl-benzamide

https://huagongshe.com/ko/reaction/968279

반응식

참여 물질

역할이름HCID투입량
반응물N-EthylanilineHCID 7670—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물2-Iodo-4-nitrobenzoic acidHCID 458964—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-ethyl-2-iodo-4-nitro-N-phenyl-benzamideHCID 2228854793%

반응 조건

온도23 °C

반응 단계

Oxalyl chloride (12 ml, 17.3 g, 0.14 mol) was added dropwise to a solution of 2-iodo-4-nitrobenzoic acid I-1 b (20 g, 68.3 mmol) in dichloromethane (137 ml). N,N-Dimethylformamide (0.1 ml) was added to the reaction mixture via syringe, the reaction mixture was stirred at 23° C. for 1 hour, and another portion of N,N-dimethylformamide (0.1 ml) was added. After stirring the reaction mixture another 2 hours, the reaction mixture was concentrated in vacuo. The residue was taken up in dichloromethane (137 ml), and DMAP (50 mg) and triethylamine (14.3 ml, 10.3 g, 0.102 mol) were added. The mixture was cooled to 0° C. and N-ethylaniline (10.1 ml, 9.9 g, 82 mmol) was added over a 10 min period. The reaction mixture was warmed to 23° C. After 16 hours at this temperature, water (150 ml) was added, and the layers were separated. The organics were washed with 1 N HCl (2 100-ml portions), dried over anhydrous sodium sulfate, and were concentrated. Purification of the residue by flash column chromatography (dichloromethane) afforded N-ethyl-2-iodo-4-nitro-N-phenyl-benzamide I-1c (24.3 g, 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06958347B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-f7c57f0be0b249669a07bf1fc0fe9b4e
출처 메모uspto-grants-2005_10