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HRID 1912882作成日:2026年10月27日

Triethylamine → 4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine

https://huagongshe.com/reaction/1912882

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Bromo-5-nitrobenzotrifluorideHCID 136198—
反応物4-EthynylpyridineHCID 642801—
触媒Copper iodideHCID 83717—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridineHCID 23155274—

反応条件

温度50 °C

反応手順

In 20 mL of dimethylformamide, 1.0 g (3.7 mmol) of 4-bromo-3-(trifluoromethyl)nitrobenzene was dissolved, and 0.502 g (3.7 mmol) of 4-ethynylpyridine, 43 mg (3 mol %) of copper iodide, 78 mg (3 mol %) of dichlorobis(triphenylphosphine)palladium and 2.06 mL (0.56 mmol) of triethylamine were added thereto and the mixture solution was stirred overnight at 50° C. in an argon atmosphere. The reaction solution was partitioned between water and ethyl acetate and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The residue was purified by a silica gel column (n-hexane:ethyl acetate=3:1) to obtain 1.3 g (quantitative) of a target product as an 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-178350c2f3cf4c4ebf09de628cdceeb6
出典メモuspto-grants-2013_12