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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1912883생성일: 2026년 10월 26일

4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine → 4-(2-Pyridin-4-yl-ethyl)-3-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1912883

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridineHCID 23155274—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매EthanolHCID 702—
생성물4-(2-Pyridin-4-yl-ethyl)-3-(trifluoromethyl)anilineHCID 2315517785%

반응 단계

In 20 mL of ethanol, 1.3 g (4.45 mmol) of 4-(4-nitro-2-(trifluoromethyl)phenylethynyl)pyridine was dissolved and stirred on 100 mg of 10% palladium carbon overnight at room temperature in a hydrogen atmosphere. The catalyst was removed by filtration and the filtrate was concentrated and the residue was purified by a silica gel column (n-hexane:ethyl acetate=1:2) to obtain 1.0 g (85%) of a target product as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609656B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-22078ad930e2479e9260fca9fb639d29
출처 메모uspto-grants-2013_12