돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270698생성일: 2026년 10월 26일

2-Aminobenzaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamide

https://huagongshe.com/reaction/270698

반응식

참여 물질

역할이름HCID투입량
반응물2-AminobenzaldehydeHCID 68255—
반응물2,6-Dichloro-3-nitrophenylacetic acidHCID 54265437—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
용매Thionyl ChlorideHCID 24386—
생성물2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamideHCID 5983388288.6%

반응 단계

A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (0.90 g, 3.35 mmol) in thionyl chloride (15 mL) is refluxed for one hour. The solvent is removed by concentration and dry toluene is added to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (30 mL) is added (drop-wise) a solution of 2-aminobenzaldehyde (0.365 g, 3.02 mmol) in dichloromethane (5.0 mL). The mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with EtOAc and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product (0.94 g, 88.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449582B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-85921cc9266e4e75939cb8df0dbc30ea
출처 메모uspto-grants-2008_11