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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1750790생성일: 2026년 10월 27일

2,2,2-Trifluoroethanol → 1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene

https://huagongshe.com/reaction/1750790

반응식

참여 물질

역할이름HCID투입량
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물Cesium carbonateHCID 10796—
반응물Ethyl 2-oxocyclohexanecarboxylateHCID 95543—
반응물Benzene, 1,3-dichloro-2-iodo-5-nitro-HCID 112948—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzeneHCID 1385222726.4%

반응 단계

A Mixture of Cs2CO3 (17.22 g, 52.84 mmol), CuBr (361 mg, 2.52 mmol) and ethyl 2-oxocyclohexanecarboxylate (856 mg, 5.03 mmol) in DMSO (30 mL) under N2 was stirred for 0.5 h at rt. Then a solution of 1,3-dichloro-2-iodo-5-nitrobenzene (8.0 g, 25.16 mmol) and 2,2,2-trifluoroethanol (3.02 g, 30.19 mmol) in DMSO (20 mL) was added to it. The reaction mixture was stirred at 80° C. for 18 h and cooled to room temperature, and then directly passed through celite. After rinsed with 250 ml of EA, the combined filter was washed by brine, dried over anhydrous Na2SO4, concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (100:1) to provide 1,3-dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene (1.93 g, yield 12.6%) as pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156860B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-9884f47841434a058d738f70ebe645ea
출처 메모uspto-grants-2015_10