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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4061생성일: 2026년 10월 23일

2,5-Dichloronitrobenzene → 5-Chloro-1-(4-chloro-2-nitrophenyl)indoline

https://huagongshe.com/ko/reaction/4061

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DichloronitrobenzeneHCID 6977—
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물5-ChloroindolineHCID 117596—
용매DimethylformamideHCID 6228—
생성물5-Chloro-1-(4-chloro-2-nitrophenyl)indolineHCID 1382332640%

반응 단계

A stirred solution of 123 g (0.80 mole) of 5-chloroindoline, 134 g (0.70 mole) of 1,4-dichloronitrobenzene and 97 g (0.80 mole) of collidine in 1000 ml of dimethylformamide was heated under nitrogen at 150° C. for 48 hours. The mixture was then cooled, filtered from some insolubles, and the solvent was removed in vacuo with warming. The residue was partitioned between 1000 ml of dichloromethane and 500 ml of water. The water layer was removed and the organic phase was washed twice with 2N-hydrochloric acid, once with 2N-sodium hydroxide, once more with water, dried over Na2SO4 and concentrated to an oil weighing 230 g. This was dissolved in 170 ml of methanol and stirred at room temperature and then at 0° C. The resultant crystals were collected, washed well with cold methanol, and dried. This afforded 86.5 g (40% yield) of product, m.p. 130°-133° C. 4 g of 5-chloro-1-(4-chloro-2-nitrophenyl)indoline were recrystallized from methanol in 85% yield (overall yield: 34%); m.p. 133°-135° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723003
출처 데이터셋uspto-grants-1988_02
ORD IDord-8616870cff044e7d82aec6c73d00f16b
출처 메모uspto-grants-1988_02