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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487912생성일: 2026년 10월 25일

Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)- → N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylaniline

https://huagongshe.com/reaction/487912

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)-HCID 67851—
반응물4-(2,4-Dichlorophenyl)-1,3-thiazol-2-amineHCID 704237—
반응물Potassium tert-butoxideHCID 23665647—
반응물Tert-butanol tetrahydrofuranHCID 66775918—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물N-[4-(2,4-Dichlorophenyl)-2-thiazolyl]-2,4-dinitro-6-trifluoromethylanilineHCID 1567171290%

반응 조건

온도20 °C

반응 단계

A solution of 7.4 g (66 mmol) of potassium tert-butylate in 50 ml of tert-butanol was added dropwise to a vigorously stirred mixture of 8.0 g (33 mmol) of 2-amino-4-(2,4-dichlorophenyl)thiazole, 9.8 g (37 mmol) of 2,4-dinitro-6-trifluoromethylchlorobenzene and 100 ml of tetrahydrofuran/tert-butanol (1:2) at 0° to 5° C. in such a way that addition was complete after 1 hour. After a further hour at 0° C., the mixture was slowly warmed, over the course of about 2 hours, to 20° C. The mixture was then adjusted to pH 4 with glacial acetic acid and diluted with about 1 l of water. The precipitate was separated off, washed with water until neutral and dried. Yield: 90%; melting point 125° to 130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298515
출처 데이터셋uspto-grants-1994_03
ORD IDord-6295631e3f164ff297119d6e328a365f
출처 메모uspto-grants-1994_03