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HRID 1912883作成日:2026年10月26日

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

https://huagongshe.com/reaction/1912883

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridineHCID 23155274—
反応物HCID 178418361HCID 178418361—
触媒HCID 178418390HCID 178418390—
溶媒EthanolHCID 702—
生成物4-(2-Pyridin-4-yl-ethyl)-3-(trifluoromethyl)anilineHCID 2315517785%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609656B2
出典データセットuspto-grants-2013_12
ORD IDord-22078ad930e2479e9260fca9fb639d29
出典メモuspto-grants-2013_12