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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1018176생성일: 2026년 10월 26일

Ammonia → 4-Amino-3,5-dichlorobenzotrifluoride

https://huagongshe.com/reaction/1018176

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Lithium fluorideHCID 224478—
반응물1,2,3-Trichloro-5-(trifluoromethyl)benzeneHCID 2733399—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-Amino-3,5-dichlorobenzotrifluorideHCID 14109472.2%

반응 조건

온도-95 °C

반응 단계

3,4,5-Trichloro-trifluoromethylbenzene (0.681 g, 2.73 mmol), lithium fluoride (7.1 mg, 0.273 mmol) and N-methylpyrrolidone (1.8 ml) are mixed in an autoclave. The autoclave is cooled to −95° C. and then ammonia (1.3 g, 76.4 mmol) is added. The autoclave is then heated at 250° C. and with stirring for 4 h and is subsequently allowed to return to room temperature. The reaction product is extracted by washing with water and with dichloromethane and then the organic phase is evaporated, after having been dried. 0.453 g (1.97 mmol) of 2,6-dichloro-4-trifluoromethylaniline is obtained with a degree of conversion of the 3,4,5-trichloro-trifluoromethylbenzene of 97%, a ratio equal to 83/17 for the selectivity for 2,6-dlchloro-para-trifluoromethylaniline with respect to 2,6-dichloro-meta-trifluoromethylaniline and an 87% yield of 2,6-dichloro-para-trifluoromethylaniline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06479703B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-6475831cd98b4b2986b7ef106e72a8e5
출처 메모uspto-grants-2002_11