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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394208생성일: 2026년 10월 26일

2,6-Dichloroaniline → Methyl 3,5-dibromo-4-{(1Z)-3-[(2,6-dichlorophenyl)amino]-3-oxoprop-1-enyl}benzoate

https://huagongshe.com/reaction/394208

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DichloroanilineHCID 11846—
반응물DiisopropylethylamineHCID 81531—
반응물Ethanedioyl dibromideHCID 84841—
반응물(2Z)-3-[2,6-Dibromo-4-(methoxycarbonyl)phenyl]prop-2-enoic acidHCID 69848595—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물Methyl 3,5-dibromo-4-{(1Z)-3-[(2,6-dichlorophenyl)amino]-3-oxoprop-1-enyl}benzoateHCID 69919937—

반응 단계

To a solution of (2Z)-3-[2,6-dibromo-4-(methoxycarbonyl)phenyl]prop-2-enoic acid (1.24 g) (contaminated with 20% of the E isomer) in dichloromethane (34 mL) at 0° C. under nitrogen atmosphere was added oxalyl bromide (2 mL of a 2M solution in dichloromethane) followed by dimethylformamide (170 μL). The mixture was then warmed to rt and stirred until all gas evolution had ceased. The reaction was cooled again to 0° C. where diisopropylethylamine (83 μL) and 2,6-dichloroaniline (607 mg) were added and the reaction warmed to rt and stirred for 16 h. The reaction mixture was then poured into brine and extracted into ethyl acetate. A small amount of unreacted starting acid was removed by washing the organic layer with saturated sodium bicarbonate solution, before drying over MgSO4 and concentrating. The residue was purified by column chromatography on silica gel to give the title compound still contaminated with 20% of the E isomer. 1H NMR (500 MHz, CDCl3): δ 8.99 (br.s, 1H, Z isomer); 8.26 (br.s, 1H, E isomer); 8.20 (s, 1H, Z isomer); 7.80-6.40 (m, 6H); 3.96 (s, 3H, E isomer); 3.92 (s, 3H, Z isomer). Mass spectrum: m/z 507 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809199B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-6e841387e3284230988fd58affca5cc9
출처 메모uspto-grants-2004_10